Canonical Allele Identifier: CA1845637135

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647858C= , CM000671.2:g.34647858C=	GRCh38
NC_000009.11:g.34647855C= , CM000671.1:g.34647855C=	GRCh37
NC_000009.10:g.34637855C=	NCBI36
NG_009029.1:g.6221C=
NG_028966.1:g.674C=
NG_009029.2:g.6270C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.355C=	ENSP00000509954.1:p.Arg119=
ENST00000378842.8:c.404C= MANE Select	ENSP00000368119.4:p.Ser135=
ENST00000378842.7:c.404C=	ENSP00000368119.3:p.Ser135=
ENST00000450095.6:c.77C=	ENSP00000401956.2:p.Ser26=
ENST00000465543.6:n.743C=
ENST00000472111.5:n.660C=
ENST00000473506.6:c.355C=	ENSP00000432839.2:p.Arg119=
ENST00000473529.5:n.540C=
ENST00000485531.1:n.845C=
ENST00000487381.5:n.789C=
ENST00000489643.6:n.283-257C=
ENST00000554085.5:c.*148C=	ENSP00000450419.1:n.*148C=
ENST00000554139.5:n.583C=
ENST00000554550.5:c.*24C=	ENSP00000451435.1:n.*24C=
ENST00000554638.5:n.876C=
ENST00000554897.5:c.*24C=	ENSP00000450942.1:n.*24C=
ENST00000554944.5:n.600C=
ENST00000555020.5:n.560C=
ENST00000555086.5:n.408C=
ENST00000555214.5:n.262-190C=
ENST00000556244.1:c.391C=
ENST00000556278.1:c.253-257C=	ENSP00000451792.1:n.253-257C=
ENST00000556494.5:n.525C=
ENST00000557541.5:n.548C=
ENST00000557706.5:n.966C=
NM_000155.3:c.404C=	NP_000146.2:p.Ser135=
NM_001258332.1:c.77C=	NP_001245261.1:p.Ser26=
NM_000155.4:c.404C= MANE Select	NP_000146.2:p.Ser135=
NM_001258332.2:c.77C=	NP_001245261.1:p.Ser26=