Canonical Allele Identifier: CA1845636245

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647528A= , CM000671.2:g.34647528A=	GRCh38
NC_000009.11:g.34647525A= , CM000671.1:g.34647525A=	GRCh37
NC_000009.10:g.34637525A=	NCBI36
NG_009029.1:g.5891A=
NG_028966.1:g.344A=
NG_009029.2:g.5940A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.289A=	ENSP00000509954.1:p.Asn97=
ENST00000378842.8:c.289A= MANE Select	ENSP00000368119.4:p.Asn97=
ENST00000378842.7:c.289A=	ENSP00000368119.3:p.Asn97=
ENST00000450095.6:c.50+270A=	ENSP00000401956.2:n.50+270A=
ENST00000465543.6:n.628A=
ENST00000472111.5:n.330A=
ENST00000473506.6:c.253-13A=	ENSP00000432839.2:n.253-13A=
ENST00000473529.5:n.336A=
ENST00000485531.1:n.515A=
ENST00000487381.5:n.548A=
ENST00000489643.6:n.282+270A=
ENST00000554085.5:c.*33A=	ENSP00000450419.1:n.*33A=
ENST00000554139.5:n.342A=
ENST00000554330.5:n.250-13A=
ENST00000554550.5:c.252+270A=	ENSP00000451435.1:n.252+270A=
ENST00000554638.5:n.546A=
ENST00000554897.5:c.252+270A=	ENSP00000450942.1:n.252+270A=
ENST00000554944.5:n.283-13A=
ENST00000555020.5:n.319A=
ENST00000555086.5:n.293A=
ENST00000555214.5:n.261+270A=
ENST00000556157.1:n.413A=
ENST00000556244.1:c.276A=
ENST00000556278.1:c.252+270A=	ENSP00000451792.1:n.252+270A=
ENST00000556403.5:n.302A=
ENST00000556494.5:n.321A=
ENST00000557541.5:n.446-13A=
ENST00000557706.5:n.636A=
NM_000155.3:c.289A=	NP_000146.2:p.Asn97=
NM_001258332.1:c.50+270A=	NP_001245261.1:n.50+270A=
NM_000155.4:c.289A= MANE Select	NP_000146.2:p.Asn97=
NM_001258332.2:c.50+270A=	NP_001245261.1:n.50+270A=