Canonical Allele Identifier: CA1845639894

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648861C= , CM000671.2:g.34648861C=	GRCh38
NC_000009.11:g.34648858C= , CM000671.1:g.34648858C=	GRCh37
NC_000009.10:g.34638858C=	NCBI36
NG_009029.1:g.7224C=
NG_028966.1:g.1677C=
NG_009029.2:g.7273C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*375C=	ENSP00000509954.1:n.*375C=
ENST00000378842.8:c.787C= MANE Select	ENSP00000368119.4:p.Arg263=
ENST00000378842.7:c.787C=	ENSP00000368119.3:p.Arg263=
ENST00000450095.6:c.460C=	ENSP00000401956.2:p.Arg154=
ENST00000473506.6:c.*375C=	ENSP00000432839.2:n.*375C=
ENST00000489643.6:n.867C=
ENST00000554085.5:c.*531C=	ENSP00000450419.1:n.*531C=
ENST00000554550.5:c.*407C=	ENSP00000451435.1:n.*407C=
ENST00000554638.5:n.1259C=
ENST00000555020.5:n.1248C=
ENST00000555086.5:n.791C=
ENST00000555754.1:n.132C=
ENST00000556244.1:c.774C=
ENST00000556278.1:c.432+405C=	ENSP00000451792.1:n.432+405C=
ENST00000557706.5:n.1349C=
NM_000155.3:c.787C=	NP_000146.2:p.Arg263=
NM_001258332.1:c.460C=	NP_001245261.1:p.Arg154=
NM_000155.4:c.787C= MANE Select	NP_000146.2:p.Arg263=
NM_001258332.2:c.460C=	NP_001245261.1:p.Arg154=