Canonical Allele Identifier: CA373284414

Gene: GALT

Linked Data

• COSMIC: COSM5683912
• MyVariant Identifiers: chr9:g.34649048A>T (hg19) ; chr9:g.34649051A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649051A>T , CM000671.2:g.34649051A>T	GRCh38
NC_000009.11:g.34649048A>T , CM000671.1:g.34649048A>T	GRCh37
NC_000009.10:g.34639048A>T	NCBI36
NG_009029.1:g.7414A>T
NG_028966.1:g.1867A>T
NG_009029.2:g.7463A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*462A>T	ENSP00000509954.1:n.*462A>T
ENST00000378842.8:c.874A>T MANE Select	ENSP00000368119.4:p.Thr292Ser
ENST00000378842.7:c.874A>T	ENSP00000368119.3:p.Thr292Ser
ENST00000450095.6:c.547A>T	ENSP00000401956.2:p.Thr183Ser
ENST00000488412.2:n.130A>T
ENST00000489643.6:n.954A>T
ENST00000554550.5:c.*494A>T	ENSP00000451435.1:n.*494A>T
ENST00000554638.5:n.1346A>T
ENST00000555020.5:n.1335A>T
ENST00000555086.5:n.981A>T
ENST00000555754.1:n.322A>T
ENST00000556278.1:c.432+595A>T	ENSP00000451792.1:n.432+595A>T
ENST00000557706.5:n.1449A>T
NM_000155.3:c.874A>T	NP_000146.2:p.Thr292Ser
NM_001258332.1:c.547A>T	NP_001245261.1:p.Thr183Ser
NM_000155.4:c.874A>T MANE Select	NP_000146.2:p.Thr292Ser
NM_001258332.2:c.547A>T	NP_001245261.1:p.Thr183Ser