Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617710A>T , CM000673.2:g.6617710A>T	GRCh38
NC_000011.9:g.6638941A>T , CM000673.1:g.6638941A>T	GRCh37
NC_000011.8:g.6595517A>T	NCBI36
NG_008653.1:g.6752T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.182T>A	ENSP00000507321.1:p.Val61Glu
ENST00000299427.12:c.296T>A MANE Select	ENSP00000299427.6:p.Val99Glu
ENST00000428886.7:n.384T>A
ENST00000436873.7:c.100T>A
ENST00000524788.2:n.1308T>A
ENST00000524903.2:n.1424T>A
ENST00000528571.6:c.*36T>A	ENSP00000434647.1:n.*36T>A
ENST00000530040.2:n.325T>A
ENST00000533371.6:c.-434T>A	ENSP00000437066.1:n.-434T>A
ENST00000534644.6:n.297T>A
ENST00000642892.1:c.-381T>A	ENSP00000494165.1:n.-381T>A
ENST00000643439.1:c.*36T>A	ENSP00000495849.1:n.*36T>A
ENST00000643479.1:n.325T>A
ENST00000643516.1:c.183T>A
ENST00000644151.1:n.1588T>A
ENST00000644218.1:c.296T>A	ENSP00000493574.1:p.Val99Glu
ENST00000644683.1:c.296T>A	ENSP00000494085.1:p.Val99Glu
ENST00000644810.1:c.230-557T>A	ENSP00000495895.1:n.230-557T>A
ENST00000644831.1:n.325T>A
ENST00000644933.1:c.-434T>A	ENSP00000496133.1:n.-434T>A
ENST00000645020.1:n.1324T>A
ENST00000645285.1:c.-434T>A	ENSP00000495058.1:n.-434T>A
ENST00000645331.1:n.318T>A
ENST00000645620.1:c.-376T>A	ENSP00000493657.1:n.-376T>A
ENST00000646777.1:n.325T>A
ENST00000647016.1:n.629T>A
ENST00000647152.1:c.-434T>A	ENSP00000495893.1:n.-434T>A
ENST00000647209.1:c.*165T>A	ENSP00000495558.1:n.*165T>A
ENST00000647346.1:n.1316T>A
ENST00000299427.10:c.296T>A	ENSP00000299427.6:p.Val99Glu
ENST00000428886.6:n.318T>A
ENST00000436873.6:c.296T>A	ENSP00000398136.2:p.Val99Glu
ENST00000528571.5:c.*36T>A	ENSP00000434647.1:n.*36T>A
ENST00000530040.1:n.408T>A
ENST00000533371.5:c.-434T>A	ENSP00000437066.1:n.-434T>A
ENST00000534644.5:n.281T>A
ENST00000611494.4:c.296T>A	ENSP00000484546.1:p.Val99Glu
NM_000391.3:c.296T>A	NP_000382.3:p.Val99Glu
NM_000391.4:c.296T>A MANE Select	NP_000382.3:p.Val99Glu

Linked Data

Genomic Alleles

Transcript Alleles