Canonical Allele Identifier: CA346166250

Gene: CGREF1 KHK

Linked Data

• MyVariant Identifiers: chr2:g.27322667C>A (hg19) ; chr2:g.27099799C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27099799C>A , CM000664.2:g.27099799C>A	GRCh38
NC_000002.11:g.27322667C>A , CM000664.1:g.27322667C>A	GRCh37
NC_000002.10:g.27176171C>A	NCBI36
NG_012199.1:g.18057C>A
NG_012199.2:g.18057C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000640154.2:c.532G>T (CGREF1)
ENST00000260599.11:c.*49C>A (KHK)	ENSP00000260599.6:n.*49C>A
ENST00000429697.2:c.*49C>A (KHK)	ENSP00000404741.2:n.*49C>A
ENST00000260598.10:c.*49C>A (KHK) MANE Select	ENSP00000260598.5:n.*49C>A
ENST00000640154.1:c.324G>T (CGREF1)	ENSP00000491464.1:p.Met108Ile
ENST00000260598.9:c.*49C>A (KHK)	ENSP00000260598.5:n.*49C>A
ENST00000260599.10:c.*49C>A (KHK)	ENSP00000260599.6:n.*49C>A
ENST00000402550.5:c.384G>T (CGREF1)	ENSP00000385103.1:p.Met128Ile
ENST00000440612.5:c.*348G>T (CGREF1)	ENSP00000394306.1:n.*348G>T
ENST00000464371.1:n.872C>A (KHK)
ENST00000490823.5:n.1294C>A (KHK)
NM_000221.2:c.*49C>A (KHK)	NP_000212.1:n.*49C>A
NM_001166240.1:c.384G>T (CGREF1)	NP_001159712.1:p.Met128Ile
NM_001301324.1:c.*62G>T (CGREF1)	NP_001288253.1:n.*62G>T
NM_006488.2:c.*49C>A (KHK)	NP_006479.1:n.*49C>A
XM_005264294.2:c.*49C>A (KHK)	XP_005264351.1:n.*49C>A
XM_005264296.2:c.*49C>A (KHK)	XP_005264353.1:n.*49C>A
XM_005264298.2:c.*49C>A (KHK)	XP_005264355.1:n.*49C>A
XM_005264294.4:c.*49C>A (KHK)	XP_005264351.1:n.*49C>A
XM_005264296.4:c.*49C>A (KHK)	XP_005264353.1:n.*49C>A
XM_005264298.4:c.*49C>A (KHK)	XP_005264355.1:n.*49C>A
XM_017004060.2:c.*49C>A (KHK)	XP_016859549.1:n.*49C>A
XM_017004061.2:c.*49C>A (KHK)	XP_016859550.1:n.*49C>A
NM_006488.3:c.*49C>A (KHK) MANE Select	NP_006479.1:n.*49C>A
NM_000221.3:c.*49C>A (KHK)	NP_000212.1:n.*49C>A
NM_001166240.2:c.384G>T (CGREF1)	NP_001159712.1:p.Met128Ile
NM_001301324.2:c.*62G>T (CGREF1)	NP_001288253.1:n.*62G>T