Canonical Allele Identifier: CA477042694
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113269891G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399169G>C , CM000673.2:g.113399169G>C GRCh38
NC_000011.9:g.113269891G>C , CM000673.1:g.113269891G>C GRCh37
NC_000011.8:g.112775101G>C NCBI36
NG_012976.1:g.16379G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303941.4:c.1200G>C MANE Select ENSP00000306678.3:p.Leu400=
ENST00000303941.3:c.1200G>C ENSP00000306678.3:p.Leu400=
NM_178510.1:c.1200G>C NP_848605.1:p.Leu400=
XM_011542736.1:c.1233G>C XP_011541038.1:p.Leu411=
XM_011542737.1:c.1203G>C XP_011541039.1:p.Leu401=
XM_011542738.1:c.1011G>C XP_011541040.1:p.Leu337=
XM_011542736.2:c.1233G>C XP_011541038.1:p.Leu411=
XM_011542737.2:c.1203G>C XP_011541039.1:p.Leu401=
XM_011542738.2:c.1011G>C XP_011541040.1:p.Leu337=
XM_017017475.1:c.1230G>C XP_016872964.1:p.Leu410=
NM_178510.2:c.1200G>C MANE Select NP_848605.1:p.Leu400=