Canonical Allele Identifier: CA464401957

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648333A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648336A>T , CM000671.2:g.34648336A>T	GRCh38
NC_000009.11:g.34648333A>T , CM000671.1:g.34648333A>T	GRCh37
NC_000009.10:g.34638333A>T	NCBI36
NG_009029.1:g.6699A>T
NG_028966.1:g.1152A>T
NG_009029.2:g.6748A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*155A>T	ENSP00000509954.1:n.*155A>T
ENST00000378842.8:c.567A>T MANE Select	ENSP00000368119.4:p.Val189=
ENST00000378842.7:c.567A>T	ENSP00000368119.3:p.Val189=
ENST00000450095.6:c.240A>T	ENSP00000401956.2:p.Val80=
ENST00000472111.5:n.823A>T
ENST00000473506.6:c.*155A>T	ENSP00000432839.2:n.*155A>T
ENST00000473529.5:n.726A>T
ENST00000485531.1:n.1161A>T
ENST00000487381.5:n.952A>T
ENST00000489643.6:n.342A>T
ENST00000554085.5:c.*311A>T	ENSP00000450419.1:n.*311A>T
ENST00000554139.5:n.813A>T
ENST00000554550.5:c.*187A>T	ENSP00000451435.1:n.*187A>T
ENST00000554638.5:n.1039A>T
ENST00000554897.5:c.*254A>T	ENSP00000450942.1:n.*254A>T
ENST00000554944.5:n.916A>T
ENST00000555020.5:n.723A>T
ENST00000555086.5:n.571A>T
ENST00000555214.5:n.388A>T
ENST00000556244.1:c.554A>T
ENST00000556278.1:c.312A>T	ENSP00000451792.1:p.Val104=
ENST00000556494.5:n.688A>T
ENST00000557706.5:n.1129A>T
NM_000155.3:c.567A>T	NP_000146.2:p.Val189=
NM_001258332.1:c.240A>T	NP_001245261.1:p.Val80=
NM_000155.4:c.567A>T MANE Select	NP_000146.2:p.Val189=
NM_001258332.2:c.240A>T	NP_001245261.1:p.Val80=