Canonical Allele Identifier: CA1139802766

Gene: LY9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160823770A= , CM000663.2:g.160823770A=	GRCh38
NC_000001.10:g.160793560A= , CM000663.1:g.160793560A=	GRCh37
NC_000001.9:g.159060184A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263285.11:c.1804A= MANE Select	ENSP00000263285.5:p.Met602=
ENST00000263285.10:c.1804A=	ENSP00000263285.5:p.Met602=
ENST00000368035.1:c.929A=
ENST00000368037.9:c.1762A=	ENSP00000357016.5:p.Met588=
ENST00000392203.8:c.1534A=	ENSP00000376039.4:p.Met512=
NM_001261456.1:c.1762A=	NP_001248385.1:p.Met588=
NM_001261457.1:c.1534A=	NP_001248386.1:p.Met512=
NM_002348.3:c.1804A=	NP_002339.2:p.Met602=
XM_011509548.1:c.1945A=	XP_011507850.1:p.Met649=
XM_011509549.1:c.1945A=	XP_011507851.1:p.Met649=
XM_011509550.1:c.1945A=	XP_011507852.1:p.Met649=
XM_011509551.1:c.1903A=	XP_011507853.1:p.Met635=
XM_011509552.1:c.1945A=	XP_011507854.1:p.Met649=
XM_011509553.1:c.1846A=	XP_011507855.1:p.Met616=
XM_011509554.1:c.1804A=	XP_011507856.1:p.Met602=
XM_011509555.1:c.1675A=	XP_011507857.1:p.Met559=
XM_011509556.1:c.1675A=	XP_011507858.1:p.Met559=
XM_011509557.1:c.1633A=	XP_011507859.1:p.Met545=
XM_011509558.1:c.1324A=	XP_011507860.1:p.Met442=
XM_011509559.1:c.1057A=	XP_011507861.1:p.Met353=
XM_011509560.1:c.1633A=	XP_011507862.1:p.Met545=
XM_017001297.1:c.1945A=	XP_016856786.1:p.Met649=
XM_017001298.1:c.1903A=	XP_016856787.1:p.Met635=
XM_017001299.1:c.1903A=	XP_016856788.1:p.Met635=
XM_017001300.1:c.1846A=	XP_016856789.1:p.Met616=
XM_017001301.1:c.1804A=	XP_016856790.1:p.Met602=
XM_017001302.1:c.1675A=	XP_016856791.1:p.Met559=
XM_017001303.1:c.1633A=	XP_016856792.1:p.Met545=
XM_017001304.1:c.1324A=	XP_016856793.1:p.Met442=
NM_002348.4:c.1804A= MANE Select	NP_002339.2:p.Met602=
NM_001261456.2:c.1762A=	NP_001248385.1:p.Met588=
NM_001261457.2:c.1534A=	NP_001248386.1:p.Met512=