Canonical Allele Identifier: CA1845641505

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649504G= , CM000671.2:g.34649504G=	GRCh38
NC_000009.11:g.34649501G= , CM000671.1:g.34649501G=	GRCh37
NC_000009.10:g.34639501G=	NCBI36
NG_009029.1:g.7867G=
NG_028966.1:g.2320G=
NG_009029.2:g.7916G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*587G=	ENSP00000509954.1:n.*587G=
ENST00000378842.8:c.999G= MANE Select	ENSP00000368119.4:p.Arg333=
ENST00000378842.7:c.999G=	ENSP00000368119.3:p.Arg333=
ENST00000450095.6:c.672G=	ENSP00000401956.2:p.Arg224=
ENST00000488412.2:n.583G=
ENST00000489643.6:n.1407G=
ENST00000554550.5:c.*619G=	ENSP00000451435.1:n.*619G=
ENST00000554638.5:n.1471G=
ENST00000555020.5:n.1788G=
ENST00000555754.1:n.447G=
ENST00000556278.1:c.432+1048G=	ENSP00000451792.1:n.432+1048G=
ENST00000557706.5:n.1574G=
NM_000155.3:c.999G=	NP_000146.2:p.Arg333=
NM_001258332.1:c.672G=	NP_001245261.1:p.Arg224=
NM_000155.4:c.999G= MANE Select	NP_000146.2:p.Arg333=
NM_001258332.2:c.672G=	NP_001245261.1:p.Arg224=