Canonical Allele Identifier: CA371277059

Gene: LYN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56010094A>T , CM000670.2:g.56010094A>T	GRCh38
NC_000008.10:g.56922653A>T , CM000670.1:g.56922653A>T	GRCh37
NC_000008.9:g.57085207A>T	NCBI36
NG_029593.1:g.135268A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002350.4:c.1523A>T MANE Select	NP_002341.1:p.Tyr508Phe
ENST00000519728.6:c.1523A>T MANE Select	ENSP00000428924.1:p.Tyr508Phe
NM_001111097.2:c.1460A>T	NP_001104567.1:p.Tyr487Phe
NM_001111097.3:c.1460A>T	NP_001104567.1:p.Tyr487Phe
NM_002350.3:c.1523A>T	NP_002341.1:p.Tyr508Phe
ENST00000519728.5:c.1523A>T	ENSP00000428924.1:p.Tyr508Phe
ENST00000520220.6:c.1460A>T	ENSP00000428424.1:p.Tyr487Phe
XM_011517529.1:c.2033A>T	XP_011515831.1:p.Tyr678Phe
XM_011517529.3:c.2033A>T	XP_011515831.1:p.Tyr678Phe
XM_011517531.1:c.1523A>T	XP_011515833.1:p.Tyr508Phe
XM_017013416.1:c.1460A>T	XP_016868905.1:p.Tyr487Phe