Canonical Allele Identifier: CA477042945
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270635T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399913T>C , CM000673.2:g.113399913T>C GRCh38
NC_000011.9:g.113270635T>C , CM000673.1:g.113270635T>C GRCh37
NC_000011.8:g.112775845T>C NCBI36
NG_012976.1:g.17123T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303941.4:c.1944T>C MANE Select ENSP00000306678.3:p.Cys648=
ENST00000303941.3:c.1944T>C ENSP00000306678.3:p.Cys648=
NM_178510.1:c.1944T>C NP_848605.1:p.Cys648=
XM_011542736.1:c.1977T>C XP_011541038.1:p.Cys659=
XM_011542737.1:c.1947T>C XP_011541039.1:p.Cys649=
XM_011542738.1:c.1755T>C XP_011541040.1:p.Cys585=
XM_011542736.2:c.1977T>C XP_011541038.1:p.Cys659=
XM_011542737.2:c.1947T>C XP_011541039.1:p.Cys649=
XM_011542738.2:c.1755T>C XP_011541040.1:p.Cys585=
XM_017017475.1:c.1974T>C XP_016872964.1:p.Cys658=
NM_178510.2:c.1944T>C MANE Select NP_848605.1:p.Cys648=