Canonical Allele Identifier: CA1845641135

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649443G= , CM000671.2:g.34649443G=	GRCh38
NC_000009.11:g.34649440G= , CM000671.1:g.34649440G=	GRCh37
NC_000009.10:g.34639440G=	NCBI36
NG_009029.1:g.7806G=
NG_028966.1:g.2259G=
NG_009029.2:g.7855G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*526G=	ENSP00000509954.1:n.*526G=
ENST00000378842.8:c.938G= MANE Select	ENSP00000368119.4:p.Trp313=
ENST00000378842.7:c.938G=	ENSP00000368119.3:p.Trp313=
ENST00000450095.6:c.611G=	ENSP00000401956.2:p.Trp204=
ENST00000488412.2:n.522G=
ENST00000489643.6:n.1346G=
ENST00000554550.5:c.*558G=	ENSP00000451435.1:n.*558G=
ENST00000554638.5:n.1410G=
ENST00000555020.5:n.1727G=
ENST00000555754.1:n.386G=
ENST00000556278.1:c.432+987G=	ENSP00000451792.1:n.432+987G=
ENST00000557706.5:n.1513G=
NM_000155.3:c.938G=	NP_000146.2:p.Trp313=
NM_001258332.1:c.611G=	NP_001245261.1:p.Trp204=
NM_000155.4:c.938G= MANE Select	NP_000146.2:p.Trp313=
NM_001258332.2:c.611G=	NP_001245261.1:p.Trp204=