Canonical Allele Identifier: CA1785777451

Gene: LYN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.55880680A= , CM000670.2:g.55880680A=	GRCh38
NC_000008.10:g.56793239A= , CM000670.1:g.56793239A=	GRCh37
NC_000008.9:g.56955793A=	NCBI36
NG_029593.1:g.5854A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519728.6:c.-6+577A= MANE Select	ENSP00000428924.1:n.-6+577A=
ENST00000519728.5:c.-6+577A=	ENSP00000428924.1:n.-6+577A=
ENST00000520220.6:c.-6+577A=	ENSP00000428424.1:n.-6+577A=
NM_001111097.2:c.-6+577A=	NP_001104567.1:n.-6+577A=
NM_002350.3:c.-6+577A=	NP_002341.1:n.-6+577A=
XM_011517529.1:c.642+577A=	XP_011515831.1:n.642+577A=
XM_011517530.1:c.642+577A=	XP_011515832.1:n.642+577A=
XR_928779.1:n.1641+577A=
XM_011517529.3:c.642+577A=	XP_011515831.1:n.642+577A=
XM_017013415.2:c.642+577A=	XP_016868904.1:n.642+577A=
NM_002350.4:c.-6+577A= MANE Select	NP_002341.1:n.-6+577A=
NM_001111097.3:c.-6+577A=	NP_001104567.1:n.-6+577A=