Canonical Allele Identifier: CA371277052

Gene: LYN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56010093T>C , CM000670.2:g.56010093T>C	GRCh38
NC_000008.10:g.56922652T>C , CM000670.1:g.56922652T>C	GRCh37
NC_000008.9:g.57085206T>C	NCBI36
NG_029593.1:g.135267T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002350.4:c.1522T>C MANE Select	NP_002341.1:p.Tyr508His
ENST00000519728.6:c.1522T>C MANE Select	ENSP00000428924.1:p.Tyr508His
NM_001111097.2:c.1459T>C	NP_001104567.1:p.Tyr487His
NM_001111097.3:c.1459T>C	NP_001104567.1:p.Tyr487His
NM_002350.3:c.1522T>C	NP_002341.1:p.Tyr508His
ENST00000519728.5:c.1522T>C	ENSP00000428924.1:p.Tyr508His
ENST00000520220.6:c.1459T>C	ENSP00000428424.1:p.Tyr487His
XM_011517529.1:c.2032T>C	XP_011515831.1:p.Tyr678His
XM_011517529.3:c.2032T>C	XP_011515831.1:p.Tyr678His
XM_011517531.1:c.1522T>C	XP_011515833.1:p.Tyr508His
XM_017013416.1:c.1459T>C	XP_016868905.1:p.Tyr487His