Canonical Allele Identifier: CA1845635481

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647163T= , CM000671.2:g.34647163T=	GRCh38
NC_000009.11:g.34647160T= , CM000671.1:g.34647160T=	GRCh37
NC_000009.10:g.34637160T=	NCBI36
NG_009029.1:g.5526T=
NG_009029.2:g.5575T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.157T=	ENSP00000509954.1:p.Trp53=
ENST00000378842.8:c.157T= MANE Select	ENSP00000368119.4:p.Trp53=
ENST00000378842.7:c.157T=	ENSP00000368119.3:p.Trp53=
ENST00000450095.6:c.-46T=	ENSP00000401956.2:n.-46T=
ENST00000465543.6:n.496T=
ENST00000468099.2:n.197T=
ENST00000472111.5:n.198T=
ENST00000473506.6:c.157T=	ENSP00000432839.2:p.Trp53=
ENST00000473529.5:n.204T=
ENST00000485531.1:n.150T=
ENST00000487381.5:n.183T=
ENST00000489643.6:n.187T=
ENST00000554085.5:c.157T=	ENSP00000450419.1:p.Trp53=
ENST00000554139.5:n.210T=
ENST00000554330.5:n.154T=
ENST00000554550.5:c.157T=	ENSP00000451435.1:p.Trp53=
ENST00000554638.5:n.181T=
ENST00000554897.5:c.157T=	ENSP00000450942.1:p.Trp53=
ENST00000554944.5:n.187T=
ENST00000555020.5:n.187T=
ENST00000555086.5:n.161T=
ENST00000555214.5:n.166T=
ENST00000556157.1:n.264T=
ENST00000556244.1:c.41T=
ENST00000556278.1:c.157T=	ENSP00000451792.1:p.Trp53=
ENST00000556403.5:n.170T=
ENST00000556494.5:n.189T=
ENST00000557541.5:n.350T=
ENST00000557706.5:n.271T=
NM_000155.3:c.157T=	NP_000146.2:p.Trp53=
NM_001258332.1:c.-46T=	NP_001245261.1:n.-46T=
NM_000155.4:c.157T= MANE Select	NP_000146.2:p.Trp53=
NM_001258332.2:c.-46T=	NP_001245261.1:n.-46T=