Canonical Allele Identifier: CA1845635671

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647205C= , CM000671.2:g.34647205C=	GRCh38
NC_000009.11:g.34647202C= , CM000671.1:g.34647202C=	GRCh37
NC_000009.10:g.34637202C=	NCBI36
NG_009029.1:g.5568C=
NG_028966.1:g.21C=
NG_009029.2:g.5617C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000155.4:c.199C= MANE Select	NP_000146.2:p.Arg67=
ENST00000378842.8:c.199C= MANE Select	ENSP00000368119.4:p.Arg67=
NM_000155.3:c.199C=	NP_000146.2:p.Arg67=
NM_001258332.1:c.-4C=	NP_001245261.1:n.-4C=
NM_001258332.2:c.-4C=	NP_001245261.1:n.-4C=
ENST00000378842.7:c.199C=	ENSP00000368119.3:p.Arg67=
ENST00000450095.6:c.-4C=	ENSP00000401956.2:n.-4C=
ENST00000465543.6:n.538C=
ENST00000468099.2:n.239C=
ENST00000472111.5:n.240C=
ENST00000473506.6:c.199C=	ENSP00000432839.2:p.Arg67=
ENST00000473529.5:n.246C=
ENST00000485531.1:n.192C=
ENST00000487381.5:n.225C=
ENST00000489643.6:n.229C=
ENST00000554085.5:c.199C=	ENSP00000450419.1:p.Arg67=
ENST00000554139.5:n.252C=
ENST00000554330.5:n.196C=
ENST00000554550.5:c.199C=	ENSP00000451435.1:p.Arg67=
ENST00000554638.5:n.223C=
ENST00000554897.5:c.199C=	ENSP00000450942.1:p.Arg67=
ENST00000554944.5:n.229C=
ENST00000555020.5:n.229C=
ENST00000555086.5:n.203C=
ENST00000555214.5:n.208C=
ENST00000556157.1:n.306C=
ENST00000556244.1:c.83C=
ENST00000556278.1:c.199C=	ENSP00000451792.1:p.Arg67=
ENST00000556403.5:n.212C=
ENST00000556494.5:n.231C=
ENST00000557541.5:n.392C=
ENST00000557706.5:n.313C=
ENST00000691183.1:c.199C=	ENSP00000509954.1:p.Arg67=