Canonical Allele Identifier: CA477043013

Gene: ANKK1

Linked Data

• MyVariant Identifiers: chr11:g.113270740A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113400018A>C , CM000673.2:g.113400018A>C	GRCh38
NC_000011.9:g.113270740A>C , CM000673.1:g.113270740A>C	GRCh37
NC_000011.8:g.112775950A>C	NCBI36
NG_012976.1:g.17228A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000303941.4:c.2049A>C MANE Select	ENSP00000306678.3:p.Ala683=
ENST00000303941.3:c.2049A>C	ENSP00000306678.3:p.Ala683=
NM_178510.1:c.2049A>C	NP_848605.1:p.Ala683=
XM_011542736.1:c.2082A>C	XP_011541038.1:p.Ala694=
XM_011542737.1:c.2052A>C	XP_011541039.1:p.Ala684=
XM_011542738.1:c.1860A>C	XP_011541040.1:p.Ala620=
XM_011542736.2:c.2082A>C	XP_011541038.1:p.Ala694=
XM_011542737.2:c.2052A>C	XP_011541039.1:p.Ala684=
XM_011542738.2:c.1860A>C	XP_011541040.1:p.Ala620=
XM_017017475.1:c.2079A>C	XP_016872964.1:p.Ala693=
NM_178510.2:c.2049A>C MANE Select	NP_848605.1:p.Ala683=