Canonical Allele Identifier: CA1845636163

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647506C= , CM000671.2:g.34647506C=	GRCh38
NC_000009.11:g.34647503C= , CM000671.1:g.34647503C=	GRCh37
NC_000009.10:g.34637503C=	NCBI36
NG_009029.1:g.5869C=
NG_028966.1:g.322C=
NG_009029.2:g.5918C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.267C=	ENSP00000509954.1:p.Tyr89=
ENST00000378842.8:c.267C= MANE Select	ENSP00000368119.4:p.Tyr89=
ENST00000378842.7:c.267C=	ENSP00000368119.3:p.Tyr89=
ENST00000450095.6:c.50+248C=	ENSP00000401956.2:n.50+248C=
ENST00000465543.6:n.606C=
ENST00000468099.2:n.540C=
ENST00000472111.5:n.308C=
ENST00000473506.6:c.253-35C=	ENSP00000432839.2:n.253-35C=
ENST00000473529.5:n.314C=
ENST00000485531.1:n.493C=
ENST00000487381.5:n.526C=
ENST00000489643.6:n.282+248C=
ENST00000554085.5:c.*11C=	ENSP00000450419.1:n.*11C=
ENST00000554139.5:n.320C=
ENST00000554330.5:n.250-35C=
ENST00000554550.5:c.252+248C=	ENSP00000451435.1:n.252+248C=
ENST00000554638.5:n.524C=
ENST00000554897.5:c.252+248C=	ENSP00000450942.1:n.252+248C=
ENST00000554944.5:n.283-35C=
ENST00000555020.5:n.297C=
ENST00000555086.5:n.271C=
ENST00000555214.5:n.261+248C=
ENST00000556157.1:n.391C=
ENST00000556244.1:c.254C=
ENST00000556278.1:c.252+248C=	ENSP00000451792.1:n.252+248C=
ENST00000556403.5:n.280C=
ENST00000556494.5:n.299C=
ENST00000557541.5:n.446-35C=
ENST00000557706.5:n.614C=
NM_000155.3:c.267C=	NP_000146.2:p.Tyr89=
NM_001258332.1:c.50+248C=	NP_001245261.1:n.50+248C=
NM_000155.4:c.267C= MANE Select	NP_000146.2:p.Tyr89=
NM_001258332.2:c.50+248C=	NP_001245261.1:n.50+248C=