Canonical Allele Identifier: CA1845639573

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648771G= , CM000671.2:g.34648771G=	GRCh38
NC_000009.11:g.34648768G= , CM000671.1:g.34648768G=	GRCh37
NC_000009.10:g.34638768G=	NCBI36
NG_009029.1:g.7134G=
NG_028966.1:g.1587G=
NG_009029.2:g.7183G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*285G=	ENSP00000509954.1:n.*285G=
ENST00000378842.8:c.697G= MANE Select	ENSP00000368119.4:p.Val233=
ENST00000378842.7:c.697G=	ENSP00000368119.3:p.Val233=
ENST00000450095.6:c.370G=	ENSP00000401956.2:p.Val124=
ENST00000473506.6:c.*285G=	ENSP00000432839.2:n.*285G=
ENST00000473529.5:n.856G=
ENST00000487381.5:n.1387G=
ENST00000489643.6:n.777G=
ENST00000554085.5:c.*441G=	ENSP00000450419.1:n.*441G=
ENST00000554550.5:c.*317G=	ENSP00000451435.1:n.*317G=
ENST00000554638.5:n.1169G=
ENST00000555020.5:n.1158G=
ENST00000555086.5:n.701G=
ENST00000555754.1:n.42G=
ENST00000556244.1:c.684G=
ENST00000556278.1:c.432+315G=	ENSP00000451792.1:n.432+315G=
ENST00000557706.5:n.1259G=
NM_000155.3:c.697G=	NP_000146.2:p.Val233=
NM_001258332.1:c.370G=	NP_001245261.1:p.Val124=
NM_000155.4:c.697G= MANE Select	NP_000146.2:p.Val233=
NM_001258332.2:c.370G=	NP_001245261.1:p.Val124=