Canonical Allele Identifier: CA6565573
Gene: ATF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.50809588C>T , CM000674.2:g.50809588C>T GRCh38
NC_000012.11:g.51203371C>T , CM000674.1:g.51203371C>T GRCh37
NC_000012.10:g.49489638C>T NCBI36
NG_027673.1:g.50583C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262053.8:c.327C>T MANE Select ENSP00000262053.3:p.Tyr109=
ENST00000262053.7:c.327C>T ENSP00000262053.3:p.Tyr109=
ENST00000551831.5:c.94-4422C>T ENSP00000448987.1:n.94-4422C>T
ENST00000552487.1:c.327C>T ENSP00000448921.1:p.Tyr109=
ENST00000552510.5:c.327C>T ENSP00000448592.1:p.Tyr109=
NM_005171.4:c.327C>T NP_005162.1:p.Tyr109=
XM_011538386.1:c.327C>T XP_011536688.1:p.Tyr109=
XM_011538387.1:c.327C>T XP_011536689.1:p.Tyr109=
XM_011538388.1:c.45C>T XP_011536690.1:p.Tyr15=
XM_011538386.2:c.327C>T XP_011536688.1:p.Tyr109=
XM_011538387.2:c.327C>T XP_011536689.1:p.Tyr109=
XM_011538388.2:c.45C>T XP_011536690.1:p.Tyr15=
XM_017019331.1:c.351C>T XP_016874820.1:p.Tyr117=
XM_017019332.1:c.327C>T XP_016874821.1:p.Tyr109=
XM_017019333.1:c.327C>T XP_016874822.1:p.Tyr109=
XM_017019334.1:c.327C>T XP_016874823.1:p.Tyr109=
XM_017019335.1:c.45C>T XP_016874824.1:p.Tyr15=
XM_017019336.1:c.45C>T XP_016874825.1:p.Tyr15=
NM_005171.5:c.327C>T MANE Select NP_005162.1:p.Tyr109=