Canonical Allele Identifier: CA1826361112

Gene: GPT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144504252C= , CM000670.2:g.144504252C=	GRCh38
NC_000008.10:g.145729635C= , CM000670.1:g.145729635C=	GRCh37
NC_000008.9:g.145700443C=	NCBI36
NG_015828.1:g.5171C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394955.3:c.-53C= MANE Select	ENSP00000378408.2:n.-53C=
ENST00000354769.8:n.113C=
ENST00000394955.2:c.-53C=	ENSP00000378408.2:n.-53C=
ENST00000527165.5:n.516C=
ENST00000527961.1:n.32C=
ENST00000528431.5:c.-4-49C=	ENSP00000433586.1:n.-4-49C=
ENST00000531330.5:n.113C=
ENST00000534702.5:n.113C=
NM_005309.2:c.-53C=	NP_005300.1:n.-53C=
XM_011516993.1:c.-4-49C=	XP_011515295.1:n.-4-49C=
XR_928744.1:n.114+713G=
XM_011516993.2:c.-4-49C=	XP_011515295.1:n.-4-49C=
XR_001746139.2:n.103+1120G=
XR_001746140.2:n.253+713G=
NM_005309.3:c.-53C= MANE Select	NP_005300.1:n.-53C=
NM_001382664.1:c.-4-49C=	NP_001369593.1:n.-4-49C=
NM_001382665.1:c.-53C=	NP_001369594.1:n.-53C=
NR_168476.1:n.113C=
NR_168477.1:n.113C=