Canonical Allele Identifier: CA1717352057
Gene: ELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74066004G= , CM000669.2:g.74066004G= GRCh38
NC_000007.13:g.73480334G= , CM000669.1:g.73480334G= GRCh37
NC_000007.12:g.73118270G= NCBI36
NG_009261.1:g.42908G=

Transcript Alleles

HGVS Amino-acid change
ENST00000692049.1:c.2272+7G= ENSP00000510104.1:n.2272+7G=
ENST00000252034.12:c.2086+7G= MANE Select ENSP00000252034.7:n.2086+7G=
ENST00000252034.11:c.2086+7G= ENSP00000252034.7:n.2086+7G=
ENST00000320399.10:c.2185+7G= ENSP00000313565.6:n.2185+7G=
ENST00000320492.11:c.1843+7G= ENSP00000315607.7:n.1843+7G=
ENST00000357036.9:c.2047+272G= ENSP00000349540.5:n.2047+272G=
ENST00000358929.8:c.2272+7G= ENSP00000351807.5:n.2272+7G=
ENST00000380553.8:c.1624+272G= ENSP00000369926.4:n.1624+272G=
ENST00000380562.8:c.2104+7G= ENSP00000369936.4:n.2104+7G=
ENST00000380575.8:c.1945+272G= ENSP00000369949.4:n.1945+272G=
ENST00000380576.9:c.2029+7G= ENSP00000369950.5:n.2029+7G=
ENST00000380584.8:c.1888+272G= ENSP00000369958.4:n.1888+272G=
ENST00000414324.5:c.2014+7G= ENSP00000392575.1:n.2014+7G=
ENST00000429192.5:c.1990+272G= ENSP00000391129.1:n.1990+272G=
ENST00000445912.5:c.2032+272G= ENSP00000389857.1:n.2032+272G=
ENST00000458204.5:c.2056+7G= ENSP00000403162.1:n.2056+7G=
ENST00000621115.4:c.1765+272G= ENSP00000480955.1:n.1765+272G=
NM_000501.3:c.2086+7G= NP_000492.2:n.2086+7G=
NM_001081752.2:c.1945+272G= NP_001075221.1:n.1945+272G=
NM_001081753.2:c.1990+272G= NP_001075222.1:n.1990+272G=
NM_001081754.2:c.2047+272G= NP_001075223.1:n.2047+272G=
NM_001081755.2:c.2029+7G= NP_001075224.1:n.2029+7G=
NM_001278912.1:c.2032+272G= NP_001265841.1:n.2032+272G=
NM_001278913.1:c.1843+7G= NP_001265842.1:n.1843+7G=
NM_001278914.1:c.2014+7G= NP_001265843.1:n.2014+7G=
NM_001278915.1:c.2104+7G= NP_001265844.1:n.2104+7G=
NM_001278916.1:c.1888+272G= NP_001265845.1:n.1888+272G=
NM_001278917.1:c.2056+7G= NP_001265846.1:n.2056+7G=
NM_001278918.1:c.1765+272G= NP_001265847.1:n.1765+272G=
NM_001278939.1:c.2272+7G= NP_001265868.1:n.2272+7G=
XM_005250187.1:c.2050+7G= XP_005250244.1:n.2050+7G=
XM_005250188.1:c.2044+7G= XP_005250245.1:n.2044+7G=
XM_011515868.1:c.2101+7G= XP_011514170.1:n.2101+7G=
XM_011515869.1:c.2071+7G= XP_011514171.1:n.2071+7G=
XM_011515870.1:c.2065+7G= XP_011514172.1:n.2065+7G=
XM_011515871.1:c.2059+7G= XP_011514173.1:n.2059+7G=
XM_011515872.1:c.2047+7G= XP_011514174.1:n.2047+7G=
XM_011515873.1:c.2044+7G= XP_011514175.1:n.2044+7G=
XM_011515874.1:c.2035+7G= XP_011514176.1:n.2035+7G=
XM_011515875.1:c.2020+7G= XP_011514177.1:n.2020+7G=
XM_011515876.1:c.2047+272G= XP_011514178.1:n.2047+272G=
XM_011515877.1:c.1990+7G= XP_011514179.1:n.1990+7G=
XM_005250187.2:c.2050+7G= XP_005250244.1:n.2050+7G=
XM_005250188.2:c.2044+7G= XP_005250245.1:n.2044+7G=
XM_011515868.2:c.2101+7G= XP_011514170.1:n.2101+7G=
XM_011515871.2:c.2059+7G= XP_011514173.1:n.2059+7G=
XM_011515872.2:c.2047+7G= XP_011514174.1:n.2047+7G=
XM_011515873.2:c.2044+7G= XP_011514175.1:n.2044+7G=
XM_011515875.2:c.2020+7G= XP_011514177.1:n.2020+7G=
XM_011515876.2:c.2047+272G= XP_011514178.1:n.2047+272G=
XM_011515877.2:c.1990+7G= XP_011514179.1:n.1990+7G=
XM_017011813.1:c.2014+7G= XP_016867302.1:n.2014+7G=
XM_017011814.2:c.2002+7G= XP_016867303.1:n.2002+7G=
NM_000501.4:c.2086+7G= MANE Select NP_000492.2:n.2086+7G=
NM_001081752.3:c.1945+272G= NP_001075221.1:n.1945+272G=
NM_001081753.3:c.1990+272G= NP_001075222.1:n.1990+272G=
NM_001081754.3:c.2047+272G= NP_001075223.1:n.2047+272G=
NM_001081755.3:c.2029+7G= NP_001075224.1:n.2029+7G=
NM_001278912.2:c.2032+272G= NP_001265841.1:n.2032+272G=
NM_001278913.2:c.1843+7G= NP_001265842.1:n.1843+7G=
NM_001278914.2:c.2014+7G= NP_001265843.1:n.2014+7G=
NM_001278915.2:c.2104+7G= NP_001265844.1:n.2104+7G=
NM_001278916.2:c.1888+272G= NP_001265845.1:n.1888+272G=
NM_001278917.2:c.2056+7G= NP_001265846.1:n.2056+7G=
NM_001278918.2:c.1765+272G= NP_001265847.1:n.1765+272G=
NM_001278939.2:c.2272+7G= NP_001265868.1:n.2272+7G=