Canonical Allele Identifier: CA1717338966
Gene: ELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74042675C= , CM000669.2:g.74042675C= GRCh38
NC_000007.13:g.73457005C= , CM000669.1:g.73457005C= GRCh37
NC_000007.12:g.73094941C= NCBI36
NG_009261.1:g.19579C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000692049.1:c.294C= ENSP00000510104.1:p.Asp98=
ENST00000252034.12:c.294C= MANE Select ENSP00000252034.7:p.Asp98=
ENST00000252034.11:c.294C= ENSP00000252034.7:p.Asp98=
ENST00000320399.10:c.294C= ENSP00000313565.6:p.Asp98=
ENST00000320492.11:c.258C= ENSP00000315607.7:p.Asp86=
ENST00000357036.9:c.294C= ENSP00000349540.5:p.Asp98=
ENST00000358929.8:c.294C= ENSP00000351807.5:p.Asp98=
ENST00000380553.8:c.232+1424C= ENSP00000369926.4:n.232+1424C=
ENST00000380562.8:c.294C= ENSP00000369936.4:p.Asp98=
ENST00000380575.8:c.264C= ENSP00000369949.4:p.Asp88=
ENST00000380576.9:c.294C= ENSP00000369950.5:p.Asp98=
ENST00000380584.8:c.294C= ENSP00000369958.4:p.Asp98=
ENST00000414324.5:c.264C= ENSP00000392575.1:p.Asp88=
ENST00000416107.5:c.*361C= ENSP00000404138.1:n.*361C=
ENST00000417091.5:c.294C= ENSP00000411092.1:p.Asp98=
ENST00000419398.1:c.42C= ENSP00000412262.1:p.Asp14=
ENST00000428787.5:c.294C= ENSP00000399499.1:p.Asp98=
ENST00000429192.5:c.294C= ENSP00000391129.1:p.Asp98=
ENST00000431562.5:c.228C= ENSP00000394549.1:p.Asp76=
ENST00000438880.5:c.197-4021C= ENSP00000389206.1:n.197-4021C=
ENST00000438906.5:c.258C= ENSP00000406949.1:p.Asp86=
ENST00000442310.5:c.294C= ENSP00000403961.1:p.Asp98=
ENST00000445912.5:c.294C= ENSP00000389857.1:p.Asp98=
ENST00000458204.5:c.264C= ENSP00000403162.1:p.Asp88=
ENST00000462506.5:n.309C=
ENST00000468517.5:n.356C=
ENST00000473323.1:n.270C=
ENST00000479432.5:n.273C=
ENST00000480728.5:n.308C=
ENST00000492003.5:n.358C=
ENST00000621115.4:c.264C= ENSP00000480955.1:p.Asp88=
NM_000501.3:c.294C= NP_000492.2:p.Asp98=
NM_001081752.2:c.264C= NP_001075221.1:p.Asp88=
NM_001081753.2:c.294C= NP_001075222.1:p.Asp98=
NM_001081754.2:c.294C= NP_001075223.1:p.Asp98=
NM_001081755.2:c.294C= NP_001075224.1:p.Asp98=
NM_001278912.1:c.294C= NP_001265841.1:p.Asp98=
NM_001278913.1:c.258C= NP_001265842.1:p.Asp86=
NM_001278914.1:c.264C= NP_001265843.1:p.Asp88=
NM_001278915.1:c.294C= NP_001265844.1:p.Asp98=
NM_001278916.1:c.294C= NP_001265845.1:p.Asp98=
NM_001278917.1:c.264C= NP_001265846.1:p.Asp88=
NM_001278918.1:c.264C= NP_001265847.1:p.Asp88=
NM_001278939.1:c.294C= NP_001265868.1:p.Asp98=
XM_005250187.1:c.258C= XP_005250244.1:p.Asp86=
XM_005250188.1:c.294C= XP_005250245.1:p.Asp98=
XM_011515868.1:c.294C= XP_011514170.1:p.Asp98=
XM_011515869.1:c.264C= XP_011514171.1:p.Asp88=
XM_011515870.1:c.258C= XP_011514172.1:p.Asp86=
XM_011515871.1:c.294C= XP_011514173.1:p.Asp98=
XM_011515872.1:c.294C= XP_011514174.1:p.Asp98=
XM_011515873.1:c.294C= XP_011514175.1:p.Asp98=
XM_011515874.1:c.228C= XP_011514176.1:p.Asp76=
XM_011515875.1:c.228C= XP_011514177.1:p.Asp76=
XM_011515876.1:c.294C= XP_011514178.1:p.Asp98=
XM_011515877.1:c.294C= XP_011514179.1:p.Asp98=
XM_005250187.2:c.258C= XP_005250244.1:p.Asp86=
XM_005250188.2:c.294C= XP_005250245.1:p.Asp98=
XM_011515868.2:c.294C= XP_011514170.1:p.Asp98=
XM_011515871.2:c.294C= XP_011514173.1:p.Asp98=
XM_011515872.2:c.294C= XP_011514174.1:p.Asp98=
XM_011515873.2:c.294C= XP_011514175.1:p.Asp98=
XM_011515875.2:c.228C= XP_011514177.1:p.Asp76=
XM_011515876.2:c.294C= XP_011514178.1:p.Asp98=
XM_011515877.2:c.294C= XP_011514179.1:p.Asp98=
XM_017011813.1:c.264C= XP_016867302.1:p.Asp88=
XM_017011814.2:c.294C= XP_016867303.1:p.Asp98=
NM_000501.4:c.294C= MANE Select NP_000492.2:p.Asp98=
NM_001081752.3:c.264C= NP_001075221.1:p.Asp88=
NM_001081753.3:c.294C= NP_001075222.1:p.Asp98=
NM_001081754.3:c.294C= NP_001075223.1:p.Asp98=
NM_001081755.3:c.294C= NP_001075224.1:p.Asp98=
NM_001278912.2:c.294C= NP_001265841.1:p.Asp98=
NM_001278913.2:c.258C= NP_001265842.1:p.Asp86=
NM_001278914.2:c.264C= NP_001265843.1:p.Asp88=
NM_001278915.2:c.294C= NP_001265844.1:p.Asp98=
NM_001278916.2:c.294C= NP_001265845.1:p.Asp98=
NM_001278917.2:c.264C= NP_001265846.1:p.Asp88=
NM_001278918.2:c.264C= NP_001265847.1:p.Asp88=
NM_001278939.2:c.294C= NP_001265868.1:p.Asp98=