Canonical Allele Identifier: CA1845640727

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649110C= , CM000671.2:g.34649110C=	GRCh38
NC_000009.11:g.34649107C= , CM000671.1:g.34649107C=	GRCh37
NC_000009.10:g.34639107C=	NCBI36
NG_009029.1:g.7473C=
NG_028966.1:g.1926C=
NG_009029.2:g.7522C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*492+29C=	ENSP00000509954.1:n.*492+29C=
ENST00000378842.8:c.904+29C= MANE Select	ENSP00000368119.4:n.904+29C=
ENST00000378842.7:c.904+29C=	ENSP00000368119.3:n.904+29C=
ENST00000450095.6:c.577+29C=	ENSP00000401956.2:n.577+29C=
ENST00000488412.2:n.189C=
ENST00000489643.6:n.1013C=
ENST00000554550.5:c.*524+29C=	ENSP00000451435.1:n.*524+29C=
ENST00000554638.5:n.1376+29C=
ENST00000555020.5:n.1394C=
ENST00000555086.5:n.1040C=
ENST00000555754.1:n.352+29C=
ENST00000556278.1:c.432+654C=	ENSP00000451792.1:n.432+654C=
ENST00000557706.5:n.1479+29C=
NM_000155.3:c.904+29C=	NP_000146.2:n.904+29C=
NM_001258332.1:c.577+29C=	NP_001245261.1:n.577+29C=
NM_000155.4:c.904+29C= MANE Select	NP_000146.2:n.904+29C=
NM_001258332.2:c.577+29C=	NP_001245261.1:n.577+29C=