Canonical Allele Identifier: CA4906588

Gene: LY6E

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143021764C>T , CM000670.2:g.143021764C>T	GRCh38
NC_000008.10:g.144103181C>T , CM000670.1:g.144103181C>T	GRCh37
NC_000008.9:g.144174556C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292494.11:c.371C>T MANE Select	ENSP00000292494.6:p.Pro124Leu
ENST00000292494.10:c.371C>T	ENSP00000292494.6:p.Pro124Leu
ENST00000429120.6:c.371C>T	ENSP00000414307.2:p.Pro124Leu
ENST00000517503.1:c.*210C>T	ENSP00000428427.2:n.*210C>T
ENST00000519546.5:c.*187C>T	ENSP00000428467.1:n.*187C>T
ENST00000519611.5:c.*187C>T	ENSP00000430796.1:n.*187C>T
ENST00000520466.5:c.371C>T	ENSP00000428572.1:p.Pro124Leu
ENST00000521003.5:c.371C>T	ENSP00000428169.1:p.Pro124Leu
ENST00000521182.5:c.*210C>T	ENSP00000430770.1:n.*210C>T
ENST00000521699.5:c.371C>T	ENSP00000427915.1:p.Pro124Leu
ENST00000522024.1:c.371C>T	ENSP00000428442.1:p.Pro124Leu
ENST00000522528.5:c.*210C>T	ENSP00000428365.1:n.*210C>T
ENST00000522971.5:c.371C>T	ENSP00000428159.1:p.Pro124Leu
ENST00000523847.5:c.172+331C>T	ENSP00000430700.1:n.172+331C>T
NM_001127213.1:c.371C>T	NP_001120685.1:p.Pro124Leu
NM_002346.2:c.371C>T	NP_002337.1:p.Pro124Leu
NM_002346.3:c.371C>T MANE Select	NP_002337.1:p.Pro124Leu
NM_001127213.2:c.371C>T	NP_001120685.1:p.Pro124Leu