Canonical Allele Identifier: CA371277040

Gene: LYN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56010090C>T , CM000670.2:g.56010090C>T	GRCh38
NC_000008.10:g.56922649C>T , CM000670.1:g.56922649C>T	GRCh37
NC_000008.9:g.57085203C>T	NCBI36
NG_029593.1:g.135264C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002350.4:c.1519C>T MANE Select	NP_002341.1:p.Gln507Ter
ENST00000519728.6:c.1519C>T MANE Select	ENSP00000428924.1:p.Gln507Ter
NM_001111097.2:c.1456C>T	NP_001104567.1:p.Gln486Ter
NM_001111097.3:c.1456C>T	NP_001104567.1:p.Gln486Ter
NM_002350.3:c.1519C>T	NP_002341.1:p.Gln507Ter
ENST00000519728.5:c.1519C>T	ENSP00000428924.1:p.Gln507Ter
ENST00000520220.6:c.1456C>T	ENSP00000428424.1:p.Gln486Ter
XM_011517529.1:c.2029C>T	XP_011515831.1:p.Gln677Ter
XM_011517529.3:c.2029C>T	XP_011515831.1:p.Gln677Ter
XM_011517531.1:c.1519C>T	XP_011515833.1:p.Gln507Ter
XM_017013416.1:c.1456C>T	XP_016868905.1:p.Gln486Ter