Canonical Allele Identifier: CA382647136

Gene: ANKK1

Linked Data

• COSMIC: COSM3981295
• MyVariant Identifiers: chr11:g.113270735C>T (hg19) ; chr11:g.113400013C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113400013C>T , CM000673.2:g.113400013C>T	GRCh38
NC_000011.9:g.113270735C>T , CM000673.1:g.113270735C>T	GRCh37
NC_000011.8:g.112775945C>T	NCBI36
NG_012976.1:g.17223C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000303941.4:c.2044C>T MANE Select	ENSP00000306678.3:p.His682Tyr
ENST00000303941.3:c.2044C>T	ENSP00000306678.3:p.His682Tyr
NM_178510.1:c.2044C>T	NP_848605.1:p.His682Tyr
XM_011542736.1:c.2077C>T	XP_011541038.1:p.His693Tyr
XM_011542737.1:c.2047C>T	XP_011541039.1:p.His683Tyr
XM_011542738.1:c.1855C>T	XP_011541040.1:p.His619Tyr
XM_011542736.2:c.2077C>T	XP_011541038.1:p.His693Tyr
XM_011542737.2:c.2047C>T	XP_011541039.1:p.His683Tyr
XM_011542738.2:c.1855C>T	XP_011541040.1:p.His619Tyr
XM_017017475.1:c.2074C>T	XP_016872964.1:p.His692Tyr
NM_178510.2:c.2044C>T MANE Select	NP_848605.1:p.His682Tyr