Canonical Allele Identifier: CA1845640982

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649381C= , CM000671.2:g.34649381C=	GRCh38
NC_000009.11:g.34649378C= , CM000671.1:g.34649378C=	GRCh37
NC_000009.10:g.34639378C=	NCBI36
NG_009029.1:g.7744C=
NG_028966.1:g.2197C=
NG_009029.2:g.7793C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*493-29C=	ENSP00000509954.1:n.*493-29C=
ENST00000378842.8:c.905-29C= MANE Select	ENSP00000368119.4:n.905-29C=
ENST00000378842.7:c.905-29C=	ENSP00000368119.3:n.905-29C=
ENST00000450095.6:c.578-29C=	ENSP00000401956.2:n.578-29C=
ENST00000488412.2:n.460C=
ENST00000489643.6:n.1284C=
ENST00000554550.5:c.*525-29C=	ENSP00000451435.1:n.*525-29C=
ENST00000554638.5:n.1377-29C=
ENST00000555020.5:n.1665C=
ENST00000555754.1:n.353-29C=
ENST00000556278.1:c.432+925C=	ENSP00000451792.1:n.432+925C=
ENST00000557706.5:n.1480-29C=
NM_000155.3:c.905-29C=	NP_000146.2:n.905-29C=
NM_001258332.1:c.578-29C=	NP_001245261.1:n.578-29C=
NM_000155.4:c.905-29C= MANE Select	NP_000146.2:n.905-29C=
NM_001258332.2:c.578-29C=	NP_001245261.1:n.578-29C=