Canonical Allele Identifier: CA2220108802

Gene: GPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.46922428G= , CM000678.2:g.46922428G=	GRCh38
NC_000016.9:g.46956340G= , CM000678.1:g.46956340G=	GRCh37
NC_000016.8:g.45513841G=	NCBI36
NG_042110.1:g.43049G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000340124.9:c.1212+12G= MANE Select	ENSP00000345282.4:n.1212+12G=
ENST00000340124.8:c.1212+12G=	ENSP00000345282.4:n.1212+12G=
ENST00000440783.2:c.912+12G=	ENSP00000413804.2:n.912+12G=
ENST00000562801.5:n.1722+12G=
NM_001142466.1:c.912+12G=	NP_001135938.1:n.912+12G=
NM_001142466.2:c.912+12G=	NP_001135938.1:n.912+12G=
NM_133443.2:c.1212+12G=	NP_597700.1:n.1212+12G=
NM_133443.3:c.1212+12G=	NP_597700.1:n.1212+12G=
XM_017023790.1:c.780+12G=	XP_016879279.1:n.780+12G=
NM_133443.4:c.1212+12G= MANE Select	NP_597700.1:n.1212+12G=
NM_001142466.3:c.912+12G=	NP_001135938.1:n.912+12G=