Canonical Allele Identifier: CA6280928

Gene: ANKK1

Linked Data

• dbSNP Id: rs2587555
• ExAC: 11:113270033 C / T
• gnomAD v2: 11-113270033-C-T
• gnomAD v4: 11-113399311-C-T
• MyVariant Identifiers: chr11:g.113270033C>T (hg19) ; chr11:g.113399311C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113399311C>T , CM000673.2:g.113399311C>T	GRCh38
NC_000011.9:g.113270033C>T , CM000673.1:g.113270033C>T	GRCh37
NC_000011.8:g.112775243C>T	NCBI36
NG_012976.1:g.16521C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303941.4:c.1342C>T MANE Select	ENSP00000306678.3:p.Leu448=
ENST00000303941.3:c.1342C>T	ENSP00000306678.3:p.Leu448=
NM_178510.1:c.1342C>T	NP_848605.1:p.Leu448=
XM_011542736.1:c.1375C>T	XP_011541038.1:p.Leu459=
XM_011542737.1:c.1345C>T	XP_011541039.1:p.Leu449=
XM_011542738.1:c.1153C>T	XP_011541040.1:p.Leu385=
XM_011542736.2:c.1375C>T	XP_011541038.1:p.Leu459=
XM_011542737.2:c.1345C>T	XP_011541039.1:p.Leu449=
XM_011542738.2:c.1153C>T	XP_011541040.1:p.Leu385=
XM_017017475.1:c.1372C>T	XP_016872964.1:p.Leu458=
NM_178510.2:c.1342C>T MANE Select	NP_848605.1:p.Leu448=