Canonical Allele Identifier: CA1845638747

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648380G= , CM000671.2:g.34648380G=	GRCh38
NC_000009.11:g.34648377G= , CM000671.1:g.34648377G=	GRCh37
NC_000009.10:g.34638377G=	NCBI36
NG_009029.1:g.6743G=
NG_028966.1:g.1196G=
NG_009029.2:g.6792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*199G=	ENSP00000509954.1:n.*199G=
ENST00000378842.8:c.611G= MANE Select	ENSP00000368119.4:p.Arg204=
ENST00000378842.7:c.611G=	ENSP00000368119.3:p.Arg204=
ENST00000450095.6:c.284G=	ENSP00000401956.2:p.Arg95=
ENST00000472111.5:n.867G=
ENST00000473506.6:c.*199G=	ENSP00000432839.2:n.*199G=
ENST00000473529.5:n.770G=
ENST00000487381.5:n.996G=
ENST00000489643.6:n.386G=
ENST00000554085.5:c.*355G=	ENSP00000450419.1:n.*355G=
ENST00000554139.5:n.857G=
ENST00000554550.5:c.*231G=	ENSP00000451435.1:n.*231G=
ENST00000554638.5:n.1083G=
ENST00000554944.5:n.960G=
ENST00000555020.5:n.767G=
ENST00000555086.5:n.615G=
ENST00000555214.5:n.432G=
ENST00000556244.1:c.598G=
ENST00000556278.1:c.356G=	ENSP00000451792.1:p.Arg119=
ENST00000556494.5:n.732G=
ENST00000557706.5:n.1173G=
NM_000155.3:c.611G=	NP_000146.2:p.Arg204=
NM_001258332.1:c.284G=	NP_001245261.1:p.Arg95=
NM_000155.4:c.611G= MANE Select	NP_000146.2:p.Arg204=
NM_001258332.2:c.284G=	NP_001245261.1:p.Arg95=