Canonical Allele Identifier: CA1261611514

Gene: HK2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74847840T= , CM000664.2:g.74847840T=	GRCh38
NC_000002.11:g.75074967T= , CM000664.1:g.75074967T=	GRCh37
NC_000002.10:g.74928475T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290573.7:c.64-6453T= MANE Select	ENSP00000290573.2:n.64-6453T=
ENST00000290573.6:c.64-6453T=	ENSP00000290573.2:n.64-6453T=
ENST00000409174.1:c.-21-6453T=	ENSP00000387140.1:n.-21-6453T=
NM_000189.4:c.64-6453T=	NP_000180.2:n.64-6453T=
XM_005264280.1:c.64-6453T=	XP_005264337.1:n.64-6453T=
XM_011532807.1:c.64-6453T=	XP_011531109.1:n.64-6453T=
XM_005264280.2:c.64-6453T=	XP_005264337.1:n.64-6453T=
XM_011532807.2:c.64-6453T=	XP_011531109.1:n.64-6453T=
XM_017003945.2:c.64-6453T=	XP_016859434.1:n.64-6453T=
NM_000189.5:c.64-6453T= MANE Select	NP_000180.2:n.64-6453T=
NM_001371525.1:c.-21-6453T=	NP_001358454.1:n.-21-6453T=