Canonical Allele Identifier: CA1845636261

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647530C= , CM000671.2:g.34647530C=	GRCh38
NC_000009.11:g.34647527C= , CM000671.1:g.34647527C=	GRCh37
NC_000009.10:g.34637527C=	NCBI36
NG_009029.1:g.5893C=
NG_028966.1:g.346C=
NG_009029.2:g.5942C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.291C=	ENSP00000509954.1:p.Asn97=
ENST00000378842.8:c.291C= MANE Select	ENSP00000368119.4:p.Asn97=
ENST00000378842.7:c.291C=	ENSP00000368119.3:p.Asn97=
ENST00000450095.6:c.50+272C=	ENSP00000401956.2:n.50+272C=
ENST00000465543.6:n.630C=
ENST00000472111.5:n.332C=
ENST00000473506.6:c.253-11C=	ENSP00000432839.2:n.253-11C=
ENST00000473529.5:n.338C=
ENST00000485531.1:n.517C=
ENST00000487381.5:n.550C=
ENST00000489643.6:n.282+272C=
ENST00000554085.5:c.*35C=	ENSP00000450419.1:n.*35C=
ENST00000554139.5:n.344C=
ENST00000554330.5:n.250-11C=
ENST00000554550.5:c.252+272C=	ENSP00000451435.1:n.252+272C=
ENST00000554638.5:n.548C=
ENST00000554897.5:c.252+272C=	ENSP00000450942.1:n.252+272C=
ENST00000554944.5:n.283-11C=
ENST00000555020.5:n.321C=
ENST00000555086.5:n.295C=
ENST00000555214.5:n.261+272C=
ENST00000556157.1:n.415C=
ENST00000556244.1:c.278C=
ENST00000556278.1:c.252+272C=	ENSP00000451792.1:n.252+272C=
ENST00000556403.5:n.304C=
ENST00000556494.5:n.323C=
ENST00000557541.5:n.446-11C=
ENST00000557706.5:n.638C=
NM_000155.3:c.291C=	NP_000146.2:p.Asn97=
NM_001258332.1:c.50+272C=	NP_001245261.1:n.50+272C=
NM_000155.4:c.291C= MANE Select	NP_000146.2:p.Asn97=
NM_001258332.2:c.50+272C=	NP_001245261.1:n.50+272C=