Canonical Allele Identifier: CA1826361172

Gene: GPT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144504344C= , CM000670.2:g.144504344C=	GRCh38
NC_000008.10:g.145729727C= , CM000670.1:g.145729727C=	GRCh37
NC_000008.9:g.145700535C=	NCBI36
NG_015828.1:g.5263C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005309.3:c.40C= MANE Select	NP_005300.1:p.His14=
ENST00000394955.3:c.40C= MANE Select	ENSP00000378408.2:p.His14=
NM_001382664.1:c.40C=	NP_001369593.1:p.His14=
NM_001382665.1:c.40C=	NP_001369594.1:p.His14=
NM_005309.2:c.40C=	NP_005300.1:p.His14=
NR_168476.1:n.205C=
NR_168477.1:n.205C=
ENST00000354769.8:n.205C=
ENST00000394955.2:c.40C=	ENSP00000378408.2:p.His14=
ENST00000527165.5:n.608C=
ENST00000527961.1:n.124C=
ENST00000528431.5:c.40C=	ENSP00000433586.1:p.His14=
ENST00000531330.5:n.205C=
ENST00000534702.5:n.205C=
XM_011516993.1:c.40C=	XP_011515295.1:p.His14=
XM_011516993.2:c.40C=	XP_011515295.1:p.His14=
XR_001746139.2:n.103+1028G=
XR_001746140.2:n.253+621G=
XR_928744.1:n.114+621G=