Canonical Allele Identifier: CA1845640955

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649350G= , CM000671.2:g.34649350G=	GRCh38
NC_000009.11:g.34649347G= , CM000671.1:g.34649347G=	GRCh37
NC_000009.10:g.34639347G=	NCBI36
NG_009029.1:g.7713G=
NG_028966.1:g.2166G=
NG_009029.2:g.7762G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*493-60G=	ENSP00000509954.1:n.*493-60G=
ENST00000378842.8:c.905-60G= MANE Select	ENSP00000368119.4:n.905-60G=
ENST00000378842.7:c.905-60G=	ENSP00000368119.3:n.905-60G=
ENST00000450095.6:c.578-60G=	ENSP00000401956.2:n.578-60G=
ENST00000488412.2:n.429G=
ENST00000489643.6:n.1253G=
ENST00000554550.5:c.*525-60G=	ENSP00000451435.1:n.*525-60G=
ENST00000554638.5:n.1377-60G=
ENST00000555020.5:n.1634G=
ENST00000555754.1:n.353-60G=
ENST00000556278.1:c.432+894G=	ENSP00000451792.1:n.432+894G=
ENST00000557706.5:n.1480-60G=
NM_000155.3:c.905-60G=	NP_000146.2:n.905-60G=
NM_001258332.1:c.578-60G=	NP_001245261.1:n.578-60G=
NM_000155.4:c.905-60G= MANE Select	NP_000146.2:n.905-60G=
NM_001258332.2:c.578-60G=	NP_001245261.1:n.578-60G=