Canonical Allele Identifier: CA6281049

Gene: ANKK1

Linked Data

• dbSNP Id: rs781581458
• ExAC: 11:113270642 G / A
• gnomAD v2: 11-113270642-G-A
• gnomAD v3: 11-113399920-G-A
• gnomAD v4: 11-113399920-G-A
• MyVariant Identifiers: chr11:g.113270642G>A (hg19) ; chr11:g.113399920G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113399920G>A , CM000673.2:g.113399920G>A	GRCh38
NC_000011.9:g.113270642G>A , CM000673.1:g.113270642G>A	GRCh37
NC_000011.8:g.112775852G>A	NCBI36
NG_012976.1:g.17130G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303941.4:c.1951G>A MANE Select	ENSP00000306678.3:p.Asp651Asn
ENST00000303941.3:c.1951G>A	ENSP00000306678.3:p.Asp651Asn
NM_178510.1:c.1951G>A	NP_848605.1:p.Asp651Asn
XM_011542736.1:c.1984G>A	XP_011541038.1:p.Asp662Asn
XM_011542737.1:c.1954G>A	XP_011541039.1:p.Asp652Asn
XM_011542738.1:c.1762G>A	XP_011541040.1:p.Asp588Asn
XM_011542736.2:c.1984G>A	XP_011541038.1:p.Asp662Asn
XM_011542737.2:c.1954G>A	XP_011541039.1:p.Asp652Asn
XM_011542738.2:c.1762G>A	XP_011541040.1:p.Asp588Asn
XM_017017475.1:c.1981G>A	XP_016872964.1:p.Asp661Asn
NM_178510.2:c.1951G>A MANE Select	NP_848605.1:p.Asp651Asn