Canonical Allele Identifier: CA371277062

Gene: LYN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56010095C>G , CM000670.2:g.56010095C>G	GRCh38
NC_000008.10:g.56922654C>G , CM000670.1:g.56922654C>G	GRCh37
NC_000008.9:g.57085208C>G	NCBI36
NG_029593.1:g.135269C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002350.4:c.1524C>G MANE Select	NP_002341.1:p.Tyr508Ter
ENST00000519728.6:c.1524C>G MANE Select	ENSP00000428924.1:p.Tyr508Ter
NM_001111097.2:c.1461C>G	NP_001104567.1:p.Tyr487Ter
NM_001111097.3:c.1461C>G	NP_001104567.1:p.Tyr487Ter
NM_002350.3:c.1524C>G	NP_002341.1:p.Tyr508Ter
ENST00000519728.5:c.1524C>G	ENSP00000428924.1:p.Tyr508Ter
ENST00000520220.6:c.1461C>G	ENSP00000428424.1:p.Tyr487Ter
XM_011517529.1:c.2034C>G	XP_011515831.1:p.Tyr678Ter
XM_011517529.3:c.2034C>G	XP_011515831.1:p.Tyr678Ter
XM_011517531.1:c.1524C>G	XP_011515833.1:p.Tyr508Ter
XM_017013416.1:c.1461C>G	XP_016868905.1:p.Tyr487Ter