Canonical Allele Identifier: CA1845639671

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648821G= , CM000671.2:g.34648821G=	GRCh38
NC_000009.11:g.34648818G= , CM000671.1:g.34648818G=	GRCh37
NC_000009.10:g.34638818G=	NCBI36
NG_009029.1:g.7184G=
NG_028966.1:g.1637G=
NG_009029.2:g.7233G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*335G=	ENSP00000509954.1:n.*335G=
ENST00000378842.8:c.747G= MANE Select	ENSP00000368119.4:p.Trp249=
ENST00000378842.7:c.747G=	ENSP00000368119.3:p.Trp249=
ENST00000450095.6:c.420G=	ENSP00000401956.2:p.Trp140=
ENST00000473506.6:c.*335G=	ENSP00000432839.2:n.*335G=
ENST00000473529.5:n.906G=
ENST00000487381.5:n.1437G=
ENST00000489643.6:n.827G=
ENST00000554085.5:c.*491G=	ENSP00000450419.1:n.*491G=
ENST00000554550.5:c.*367G=	ENSP00000451435.1:n.*367G=
ENST00000554638.5:n.1219G=
ENST00000555020.5:n.1208G=
ENST00000555086.5:n.751G=
ENST00000555754.1:n.92G=
ENST00000556244.1:c.734G=
ENST00000556278.1:c.432+365G=	ENSP00000451792.1:n.432+365G=
ENST00000557706.5:n.1309G=
NM_000155.3:c.747G=	NP_000146.2:p.Trp249=
NM_001258332.1:c.420G=	NP_001245261.1:p.Trp140=
NM_000155.4:c.747G= MANE Select	NP_000146.2:p.Trp249=
NM_001258332.2:c.420G=	NP_001245261.1:p.Trp140=