Canonical Allele Identifier: CA1845639928

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648865T= , CM000671.2:g.34648865T=	GRCh38
NC_000009.11:g.34648862T= , CM000671.1:g.34648862T=	GRCh37
NC_000009.10:g.34638862T=	NCBI36
NG_009029.1:g.7228T=
NG_028966.1:g.1681T=
NG_009029.2:g.7277T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*379T=	ENSP00000509954.1:n.*379T=
ENST00000378842.8:c.791T= MANE Select	ENSP00000368119.4:p.Leu264=
ENST00000378842.7:c.791T=	ENSP00000368119.3:p.Leu264=
ENST00000450095.6:c.464T=	ENSP00000401956.2:p.Leu155=
ENST00000473506.6:c.*379T=	ENSP00000432839.2:n.*379T=
ENST00000489643.6:n.871T=
ENST00000554085.5:c.*535T=	ENSP00000450419.1:n.*535T=
ENST00000554550.5:c.*411T=	ENSP00000451435.1:n.*411T=
ENST00000554638.5:n.1263T=
ENST00000555020.5:n.1252T=
ENST00000555086.5:n.795T=
ENST00000555754.1:n.136T=
ENST00000556244.1:c.778T=
ENST00000556278.1:c.432+409T=	ENSP00000451792.1:n.432+409T=
ENST00000557706.5:n.1353T=
NM_000155.3:c.791T=	NP_000146.2:p.Leu264=
NM_001258332.1:c.464T=	NP_001245261.1:p.Leu155=
NM_000155.4:c.791T= MANE Select	NP_000146.2:p.Leu264=
NM_001258332.2:c.464T=	NP_001245261.1:p.Leu155=