Canonical Allele Identifier: CA1845636417

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647632A= , CM000671.2:g.34647632A=	GRCh38
NC_000009.11:g.34647629A= , CM000671.1:g.34647629A=	GRCh37
NC_000009.10:g.34637629A=	NCBI36
NG_009029.1:g.5995A=
NG_028966.1:g.448A=
NG_009029.2:g.6044A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+65A=	ENSP00000509954.1:n.328+65A=
ENST00000378842.8:c.329-25A= MANE Select	ENSP00000368119.4:n.329-25A=
ENST00000378842.7:c.329-25A=	ENSP00000368119.3:n.329-25A=
ENST00000450095.6:c.51-200A=	ENSP00000401956.2:n.51-200A=
ENST00000465543.6:n.668-25A=
ENST00000472111.5:n.434A=
ENST00000473506.6:c.280-25A=	ENSP00000432839.2:n.280-25A=
ENST00000473529.5:n.440A=
ENST00000485531.1:n.619A=
ENST00000487381.5:n.588-25A=
ENST00000489643.6:n.282+374A=
ENST00000554085.5:c.*73-25A=	ENSP00000450419.1:n.*73-25A=
ENST00000554139.5:n.382-25A=
ENST00000554330.5:n.341A=
ENST00000554550.5:c.253-200A=	ENSP00000451435.1:n.253-200A=
ENST00000554638.5:n.650A=
ENST00000554897.5:c.253-200A=	ENSP00000450942.1:n.253-200A=
ENST00000554944.5:n.374A=
ENST00000555020.5:n.359-25A=
ENST00000555086.5:n.333-25A=
ENST00000555214.5:n.261+374A=
ENST00000556157.1:n.453-25A=
ENST00000556244.1:c.316-25A=
ENST00000556278.1:c.252+374A=	ENSP00000451792.1:n.252+374A=
ENST00000556403.5:n.406A=
ENST00000556494.5:n.425A=
ENST00000557541.5:n.473-25A=
ENST00000557706.5:n.740A=
NM_000155.3:c.329-25A=	NP_000146.2:n.329-25A=
NM_001258332.1:c.51-200A=	NP_001245261.1:n.51-200A=
NM_000155.4:c.329-25A= MANE Select	NP_000146.2:n.329-25A=
NM_001258332.2:c.51-200A=	NP_001245261.1:n.51-200A=