Canonical Allele Identifier: CA1845638870

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648403C= , CM000671.2:g.34648403C=	GRCh38
NC_000009.11:g.34648400C= , CM000671.1:g.34648400C=	GRCh37
NC_000009.10:g.34638400C=	NCBI36
NG_009029.1:g.6766C=
NG_028966.1:g.1219C=
NG_009029.2:g.6815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*222C=	ENSP00000509954.1:n.*222C=
ENST00000378842.8:c.634C= MANE Select	ENSP00000368119.4:p.Gln212=
ENST00000378842.7:c.634C=	ENSP00000368119.3:p.Gln212=
ENST00000450095.6:c.307C=	ENSP00000401956.2:p.Gln103=
ENST00000472111.5:n.890C=
ENST00000473506.6:c.*222C=	ENSP00000432839.2:n.*222C=
ENST00000473529.5:n.793C=
ENST00000487381.5:n.1019C=
ENST00000489643.6:n.409C=
ENST00000554085.5:c.*378C=	ENSP00000450419.1:n.*378C=
ENST00000554550.5:c.*254C=	ENSP00000451435.1:n.*254C=
ENST00000554638.5:n.1106C=
ENST00000555020.5:n.790C=
ENST00000555086.5:n.638C=
ENST00000555214.5:n.455C=
ENST00000556244.1:c.621C=
ENST00000556278.1:c.379C=	ENSP00000451792.1:p.Gln127=
ENST00000556494.5:n.755C=
ENST00000557706.5:n.1196C=
NM_000155.3:c.634C=	NP_000146.2:p.Gln212=
NM_001258332.1:c.307C=	NP_001245261.1:p.Gln103=
NM_000155.4:c.634C= MANE Select	NP_000146.2:p.Gln212=
NM_001258332.2:c.307C=	NP_001245261.1:p.Gln103=