Canonical Allele Identifier: CA160131367
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 523433
dbSNP Id: rs766735416
gnomAD v2: 7-73466262-A-T
gnomAD v3: 7-74051932-A-T
gnomAD v4: 7-74051932-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74051932A>T , CM000669.2:g.74051932A>T GRCh38
NC_000007.13:g.73466262A>T , CM000669.1:g.73466262A>T GRCh37
NC_000007.12:g.73104198A>T NCBI36
NG_009261.1:g.28836A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000692049.1:c.898A>T ENSP00000510104.1:p.Thr300Ser
ENST00000252034.12:c.898A>T MANE Select ENSP00000252034.7:p.Thr300Ser
ENST00000252034.11:c.898A>T ENSP00000252034.7:p.Thr300Ser
ENST00000320399.10:c.898A>T ENSP00000313565.6:p.Thr300Ser
ENST00000320492.11:c.790A>T ENSP00000315607.7:p.Thr264Ser
ENST00000357036.9:c.913A>T ENSP00000349540.5:p.Thr305Ser
ENST00000358929.8:c.898A>T ENSP00000351807.5:p.Thr300Ser
ENST00000380553.8:c.547A>T ENSP00000369926.4:p.Thr183Ser
ENST00000380562.8:c.898A>T ENSP00000369936.4:p.Thr300Ser
ENST00000380575.8:c.868A>T ENSP00000369949.4:p.Thr290Ser
ENST00000380576.9:c.898A>T ENSP00000369950.5:p.Thr300Ser
ENST00000380584.8:c.856A>T ENSP00000369958.4:p.Thr286Ser
ENST00000414324.5:c.883A>T ENSP00000392575.1:p.Thr295Ser
ENST00000429192.5:c.913A>T ENSP00000391129.1:p.Thr305Ser
ENST00000438880.5:c.481A>T ENSP00000389206.1:p.Thr161Ser
ENST00000438906.5:c.832A>T ENSP00000406949.1:p.Thr278Ser
ENST00000445912.5:c.898A>T ENSP00000389857.1:p.Thr300Ser
ENST00000458204.5:c.868A>T ENSP00000403162.1:p.Thr290Ser
ENST00000493839.1:n.448A>T
ENST00000621115.4:c.766A>T ENSP00000480955.1:p.Thr256Ser
NM_000501.3:c.898A>T NP_000492.2:p.Thr300Ser
NM_001081752.2:c.868A>T NP_001075221.1:p.Thr290Ser
NM_001081753.2:c.913A>T NP_001075222.1:p.Thr305Ser
NM_001081754.2:c.913A>T NP_001075223.1:p.Thr305Ser
NM_001081755.2:c.898A>T NP_001075224.1:p.Thr300Ser
NM_001278912.1:c.898A>T NP_001265841.1:p.Thr300Ser
NM_001278913.1:c.790A>T NP_001265842.1:p.Thr264Ser
NM_001278914.1:c.883A>T NP_001265843.1:p.Thr295Ser
NM_001278915.1:c.898A>T NP_001265844.1:p.Thr300Ser
NM_001278916.1:c.856A>T NP_001265845.1:p.Thr286Ser
NM_001278917.1:c.868A>T NP_001265846.1:p.Thr290Ser
NM_001278918.1:c.766A>T NP_001265847.1:p.Thr256Ser
NM_001278939.1:c.898A>T NP_001265868.1:p.Thr300Ser
XM_005250187.1:c.862A>T XP_005250244.1:p.Thr288Ser
XM_005250188.1:c.856A>T XP_005250245.1:p.Thr286Ser
XM_011515868.1:c.913A>T XP_011514170.1:p.Thr305Ser
XM_011515869.1:c.883A>T XP_011514171.1:p.Thr295Ser
XM_011515870.1:c.877A>T XP_011514172.1:p.Thr293Ser
XM_011515871.1:c.871A>T XP_011514173.1:p.Thr291Ser
XM_011515872.1:c.913A>T XP_011514174.1:p.Thr305Ser
XM_011515873.1:c.913A>T XP_011514175.1:p.Thr305Ser
XM_011515874.1:c.847A>T XP_011514176.1:p.Thr283Ser
XM_011515875.1:c.832A>T XP_011514177.1:p.Thr278Ser
XM_011515876.1:c.913A>T XP_011514178.1:p.Thr305Ser
XM_011515877.1:c.913A>T XP_011514179.1:p.Thr305Ser
XM_005250187.2:c.862A>T XP_005250244.1:p.Thr288Ser
XM_005250188.2:c.856A>T XP_005250245.1:p.Thr286Ser
XM_011515868.2:c.913A>T XP_011514170.1:p.Thr305Ser
XM_011515871.2:c.871A>T XP_011514173.1:p.Thr291Ser
XM_011515872.2:c.913A>T XP_011514174.1:p.Thr305Ser
XM_011515873.2:c.913A>T XP_011514175.1:p.Thr305Ser
XM_011515875.2:c.832A>T XP_011514177.1:p.Thr278Ser
XM_011515876.2:c.913A>T XP_011514178.1:p.Thr305Ser
XM_011515877.2:c.913A>T XP_011514179.1:p.Thr305Ser
XM_017011813.1:c.826A>T XP_016867302.1:p.Thr276Ser
XM_017011814.2:c.871A>T XP_016867303.1:p.Thr291Ser
NM_000501.4:c.898A>T MANE Select NP_000492.2:p.Thr300Ser
NM_001081752.3:c.868A>T NP_001075221.1:p.Thr290Ser
NM_001081753.3:c.913A>T NP_001075222.1:p.Thr305Ser
NM_001081754.3:c.913A>T NP_001075223.1:p.Thr305Ser
NM_001081755.3:c.898A>T NP_001075224.1:p.Thr300Ser
NM_001278912.2:c.898A>T NP_001265841.1:p.Thr300Ser
NM_001278913.2:c.790A>T NP_001265842.1:p.Thr264Ser
NM_001278914.2:c.883A>T NP_001265843.1:p.Thr295Ser
NM_001278915.2:c.898A>T NP_001265844.1:p.Thr300Ser
NM_001278916.2:c.856A>T NP_001265845.1:p.Thr286Ser
NM_001278917.2:c.868A>T NP_001265846.1:p.Thr290Ser
NM_001278918.2:c.766A>T NP_001265847.1:p.Thr256Ser
NM_001278939.2:c.898A>T NP_001265868.1:p.Thr300Ser