Canonical Allele Identifier: CA1826361116

Gene: GPT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144504258G= , CM000670.2:g.144504258G=	GRCh38
NC_000008.10:g.145729641G= , CM000670.1:g.145729641G=	GRCh37
NC_000008.9:g.145700449G=	NCBI36
NG_015828.1:g.5177G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394955.3:c.-47G= MANE Select	ENSP00000378408.2:n.-47G=
ENST00000354769.8:n.119G=
ENST00000394955.2:c.-47G=	ENSP00000378408.2:n.-47G=
ENST00000527165.5:n.522G=
ENST00000527961.1:n.38G=
ENST00000528431.5:c.-4-43G=	ENSP00000433586.1:n.-4-43G=
ENST00000531330.5:n.119G=
ENST00000534702.5:n.119G=
NM_005309.2:c.-47G=	NP_005300.1:n.-47G=
XM_011516993.1:c.-4-43G=	XP_011515295.1:n.-4-43G=
XR_928744.1:n.114+707C=
XM_011516993.2:c.-4-43G=	XP_011515295.1:n.-4-43G=
XR_001746139.2:n.103+1114C=
XR_001746140.2:n.253+707C=
NM_005309.3:c.-47G= MANE Select	NP_005300.1:n.-47G=
NM_001382664.1:c.-4-43G=	NP_001369593.1:n.-4-43G=
NM_001382665.1:c.-47G=	NP_001369594.1:n.-47G=
NR_168476.1:n.119G=
NR_168477.1:n.119G=