Canonical Allele Identifier: CA1826361123

Gene: GPT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144504270C= , CM000670.2:g.144504270C=	GRCh38
NC_000008.10:g.145729653C= , CM000670.1:g.145729653C=	GRCh37
NC_000008.9:g.145700461C=	NCBI36
NG_015828.1:g.5189C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394955.3:c.-35C= MANE Select	ENSP00000378408.2:n.-35C=
ENST00000354769.8:n.131C=
ENST00000394955.2:c.-35C=	ENSP00000378408.2:n.-35C=
ENST00000527165.5:n.534C=
ENST00000527961.1:n.50C=
ENST00000528431.5:c.-4-31C=	ENSP00000433586.1:n.-4-31C=
ENST00000531330.5:n.131C=
ENST00000534702.5:n.131C=
NM_005309.2:c.-35C=	NP_005300.1:n.-35C=
XM_011516993.1:c.-4-31C=	XP_011515295.1:n.-4-31C=
XR_928744.1:n.114+695G=
XM_011516993.2:c.-4-31C=	XP_011515295.1:n.-4-31C=
XR_001746139.2:n.103+1102G=
XR_001746140.2:n.253+695G=
NM_005309.3:c.-35C= MANE Select	NP_005300.1:n.-35C=
NM_001382664.1:c.-4-31C=	NP_001369593.1:n.-4-31C=
NM_001382665.1:c.-35C=	NP_001369594.1:n.-35C=
NR_168476.1:n.131C=
NR_168477.1:n.131C=