Canonical Allele Identifier: CA1845638778

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648385C= , CM000671.2:g.34648385C=	GRCh38
NC_000009.11:g.34648382C= , CM000671.1:g.34648382C=	GRCh37
NC_000009.10:g.34638382C=	NCBI36
NG_009029.1:g.6748C=
NG_028966.1:g.1201C=
NG_009029.2:g.6797C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*204C=	ENSP00000509954.1:n.*204C=
ENST00000378842.8:c.616C= MANE Select	ENSP00000368119.4:p.Gln206=
ENST00000378842.7:c.616C=	ENSP00000368119.3:p.Gln206=
ENST00000450095.6:c.289C=	ENSP00000401956.2:p.Gln97=
ENST00000472111.5:n.872C=
ENST00000473506.6:c.*204C=	ENSP00000432839.2:n.*204C=
ENST00000473529.5:n.775C=
ENST00000487381.5:n.1001C=
ENST00000489643.6:n.391C=
ENST00000554085.5:c.*360C=	ENSP00000450419.1:n.*360C=
ENST00000554550.5:c.*236C=	ENSP00000451435.1:n.*236C=
ENST00000554638.5:n.1088C=
ENST00000554944.5:n.965C=
ENST00000555020.5:n.772C=
ENST00000555086.5:n.620C=
ENST00000555214.5:n.437C=
ENST00000556244.1:c.603C=
ENST00000556278.1:c.361C=	ENSP00000451792.1:p.Gln121=
ENST00000556494.5:n.737C=
ENST00000557706.5:n.1178C=
NM_000155.3:c.616C=	NP_000146.2:p.Gln206=
NM_001258332.1:c.289C=	NP_001245261.1:p.Gln97=
NM_000155.4:c.616C= MANE Select	NP_000146.2:p.Gln206=
NM_001258332.2:c.289C=	NP_001245261.1:p.Gln97=