Canonical Allele Identifier: CA1845639620

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648779C= , CM000671.2:g.34648779C=	GRCh38
NC_000009.11:g.34648776C= , CM000671.1:g.34648776C=	GRCh37
NC_000009.10:g.34638776C=	NCBI36
NG_009029.1:g.7142C=
NG_028966.1:g.1595C=
NG_009029.2:g.7191C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*293C=	ENSP00000509954.1:n.*293C=
ENST00000378842.8:c.705C= MANE Select	ENSP00000368119.4:p.Thr235=
ENST00000378842.7:c.705C=	ENSP00000368119.3:p.Thr235=
ENST00000450095.6:c.378C=	ENSP00000401956.2:p.Thr126=
ENST00000473506.6:c.*293C=	ENSP00000432839.2:n.*293C=
ENST00000473529.5:n.864C=
ENST00000487381.5:n.1395C=
ENST00000489643.6:n.785C=
ENST00000554085.5:c.*449C=	ENSP00000450419.1:n.*449C=
ENST00000554550.5:c.*325C=	ENSP00000451435.1:n.*325C=
ENST00000554638.5:n.1177C=
ENST00000555020.5:n.1166C=
ENST00000555086.5:n.709C=
ENST00000555754.1:n.50C=
ENST00000556244.1:c.692C=
ENST00000556278.1:c.432+323C=	ENSP00000451792.1:n.432+323C=
ENST00000557706.5:n.1267C=
NM_000155.3:c.705C=	NP_000146.2:p.Thr235=
NM_001258332.1:c.378C=	NP_001245261.1:p.Thr126=
NM_000155.4:c.705C= MANE Select	NP_000146.2:p.Thr235=
NM_001258332.2:c.378C=	NP_001245261.1:p.Thr126=