Canonical Allele Identifier: CA1845636450

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647645C= , CM000671.2:g.34647645C=	GRCh38
NC_000009.11:g.34647642C= , CM000671.1:g.34647642C=	GRCh37
NC_000009.10:g.34637642C=	NCBI36
NG_009029.1:g.6008C=
NG_028966.1:g.461C=
NG_009029.2:g.6057C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+78C=	ENSP00000509954.1:n.328+78C=
ENST00000378842.8:c.329-12C= MANE Select	ENSP00000368119.4:n.329-12C=
ENST00000378842.7:c.329-12C=	ENSP00000368119.3:n.329-12C=
ENST00000450095.6:c.51-187C=	ENSP00000401956.2:n.51-187C=
ENST00000465543.6:n.668-12C=
ENST00000472111.5:n.447C=
ENST00000473506.6:c.280-12C=	ENSP00000432839.2:n.280-12C=
ENST00000473529.5:n.453C=
ENST00000485531.1:n.632C=
ENST00000487381.5:n.588-12C=
ENST00000489643.6:n.282+387C=
ENST00000554085.5:c.*73-12C=	ENSP00000450419.1:n.*73-12C=
ENST00000554139.5:n.382-12C=
ENST00000554330.5:n.354C=
ENST00000554550.5:c.253-187C=	ENSP00000451435.1:n.253-187C=
ENST00000554638.5:n.663C=
ENST00000554897.5:c.253-187C=	ENSP00000450942.1:n.253-187C=
ENST00000554944.5:n.387C=
ENST00000555020.5:n.359-12C=
ENST00000555086.5:n.333-12C=
ENST00000555214.5:n.261+387C=
ENST00000556157.1:n.453-12C=
ENST00000556244.1:c.316-12C=
ENST00000556278.1:c.252+387C=	ENSP00000451792.1:n.252+387C=
ENST00000556403.5:n.419C=
ENST00000556494.5:n.438C=
ENST00000557541.5:n.473-12C=
ENST00000557706.5:n.753C=
NM_000155.3:c.329-12C=	NP_000146.2:n.329-12C=
NM_001258332.1:c.51-187C=	NP_001245261.1:n.51-187C=
NM_000155.4:c.329-12C= MANE Select	NP_000146.2:n.329-12C=
NM_001258332.2:c.51-187C=	NP_001245261.1:n.51-187C=