Canonical Allele Identifier: CA2581779621

Gene: HK2

Genomic Alleles

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

Transcript Alleles

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