Canonical Allele Identifier: CA2035762034

Gene: ATF1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50819982T= , CM000674.2:g.50819982T=	GRCh38
NC_000012.11:g.51213765T= , CM000674.1:g.51213765T=	GRCh37
NC_000012.10:g.49500032T=	NCBI36
NG_027673.1:g.60977T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262053.8:c.*203T= MANE Select	ENSP00000262053.3:n.*203T=
ENST00000262053.7:c.*203T=	ENSP00000262053.3:n.*203T=
ENST00000551831.5:c.*616T=	ENSP00000448987.1:n.*616T=
NM_005171.4:c.*203T=	NP_005162.1:n.*203T=
XM_011538386.1:c.*203T=	XP_011536688.1:n.*203T=
XM_011538387.1:c.*203T=	XP_011536689.1:n.*203T=
XM_011538388.1:c.*203T=	XP_011536690.1:n.*203T=
XM_011538386.2:c.*203T=	XP_011536688.1:n.*203T=
XM_011538387.2:c.*203T=	XP_011536689.1:n.*203T=
XM_011538388.2:c.*203T=	XP_011536690.1:n.*203T=
XM_017019331.1:c.*203T=	XP_016874820.1:n.*203T=
XM_017019332.1:c.*203T=	XP_016874821.1:n.*203T=
XM_017019333.1:c.*203T=	XP_016874822.1:n.*203T=
XM_017019334.1:c.*203T=	XP_016874823.1:n.*203T=
XM_017019335.1:c.*203T=	XP_016874824.1:n.*203T=
XM_017019336.1:c.*203T=	XP_016874825.1:n.*203T=
NM_005171.5:c.*203T= MANE Select	NP_005162.1:n.*203T=