Canonical Allele Identifier: CA1845636754

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647746T= , CM000671.2:g.34647746T=	GRCh38
NC_000009.11:g.34647743T= , CM000671.1:g.34647743T=	GRCh37
NC_000009.10:g.34637743T=	NCBI36
NG_009029.1:g.6109T=
NG_028966.1:g.562T=
NG_009029.2:g.6158T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.329-86T=	ENSP00000509954.1:n.329-86T=
ENST00000378842.8:c.377+41T= MANE Select	ENSP00000368119.4:n.377+41T=
ENST00000378842.7:c.377+41T=	ENSP00000368119.3:n.377+41T=
ENST00000450095.6:c.51-86T=	ENSP00000401956.2:n.51-86T=
ENST00000465543.6:n.716+41T=
ENST00000472111.5:n.548T=
ENST00000473506.6:c.328+41T=	ENSP00000432839.2:n.328+41T=
ENST00000473529.5:n.513+41T=
ENST00000485531.1:n.733T=
ENST00000487381.5:n.677T=
ENST00000489643.6:n.283-369T=
ENST00000554085.5:c.*121+41T=	ENSP00000450419.1:n.*121+41T=
ENST00000554139.5:n.471T=
ENST00000554330.5:n.455T=
ENST00000554550.5:c.253-86T=	ENSP00000451435.1:n.253-86T=
ENST00000554638.5:n.764T=
ENST00000554897.5:c.253-86T=	ENSP00000450942.1:n.253-86T=
ENST00000554944.5:n.488T=
ENST00000555020.5:n.448T=
ENST00000555086.5:n.381+41T=
ENST00000555214.5:n.262-302T=
ENST00000556157.1:n.542T=
ENST00000556244.1:c.364+41T=
ENST00000556278.1:c.253-369T=	ENSP00000451792.1:n.253-369T=
ENST00000556403.5:n.520T=
ENST00000556494.5:n.498+41T=
ENST00000557541.5:n.521+41T=
ENST00000557706.5:n.854T=
NM_000155.3:c.377+41T=	NP_000146.2:n.377+41T=
NM_001258332.1:c.51-86T=	NP_001245261.1:n.51-86T=
NM_000155.4:c.377+41T= MANE Select	NP_000146.2:n.377+41T=
NM_001258332.2:c.51-86T=	NP_001245261.1:n.51-86T=