Canonical Allele Identifier: CA1845639995

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648879C= , CM000671.2:g.34648879C=	GRCh38
NC_000009.11:g.34648876C= , CM000671.1:g.34648876C=	GRCh37
NC_000009.10:g.34638876C=	NCBI36
NG_009029.1:g.7242C=
NG_028966.1:g.1695C=
NG_009029.2:g.7291C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*393C=	ENSP00000509954.1:n.*393C=
ENST00000378842.8:c.805C= MANE Select	ENSP00000368119.4:p.Pro269=
ENST00000378842.7:c.805C=	ENSP00000368119.3:p.Pro269=
ENST00000450095.6:c.478C=	ENSP00000401956.2:p.Pro160=
ENST00000473506.6:c.*393C=	ENSP00000432839.2:n.*393C=
ENST00000489643.6:n.885C=
ENST00000554085.5:c.*549C=	ENSP00000450419.1:n.*549C=
ENST00000554550.5:c.*425C=	ENSP00000451435.1:n.*425C=
ENST00000554638.5:n.1277C=
ENST00000555020.5:n.1266C=
ENST00000555086.5:n.809C=
ENST00000555754.1:n.150C=
ENST00000556244.1:c.792C=
ENST00000556278.1:c.432+423C=	ENSP00000451792.1:n.432+423C=
ENST00000557706.5:n.1367C=
NM_000155.3:c.805C=	NP_000146.2:p.Pro269=
NM_001258332.1:c.478C=	NP_001245261.1:p.Pro160=
NM_000155.4:c.805C= MANE Select	NP_000146.2:p.Pro269=
NM_001258332.2:c.478C=	NP_001245261.1:p.Pro160=