Canonical Allele Identifier: CA464403302

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648875C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648878C>G , CM000671.2:g.34648878C>G	GRCh38
NC_000009.11:g.34648875C>G , CM000671.1:g.34648875C>G	GRCh37
NC_000009.10:g.34638875C>G	NCBI36
NG_009029.1:g.7241C>G
NG_028966.1:g.1694C>G
NG_009029.2:g.7290C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*392C>G	ENSP00000509954.1:n.*392C>G
ENST00000378842.8:c.804C>G MANE Select	ENSP00000368119.4:p.Thr268=
ENST00000378842.7:c.804C>G	ENSP00000368119.3:p.Thr268=
ENST00000450095.6:c.477C>G	ENSP00000401956.2:p.Thr159=
ENST00000473506.6:c.*392C>G	ENSP00000432839.2:n.*392C>G
ENST00000489643.6:n.884C>G
ENST00000554085.5:c.*548C>G	ENSP00000450419.1:n.*548C>G
ENST00000554550.5:c.*424C>G	ENSP00000451435.1:n.*424C>G
ENST00000554638.5:n.1276C>G
ENST00000555020.5:n.1265C>G
ENST00000555086.5:n.808C>G
ENST00000555754.1:n.149C>G
ENST00000556244.1:c.791C>G
ENST00000556278.1:c.432+422C>G	ENSP00000451792.1:n.432+422C>G
ENST00000557706.5:n.1366C>G
NM_000155.3:c.804C>G	NP_000146.2:p.Thr268=
NM_001258332.1:c.477C>G	NP_001245261.1:p.Thr159=
NM_000155.4:c.804C>G MANE Select	NP_000146.2:p.Thr268=
NM_001258332.2:c.477C>G	NP_001245261.1:p.Thr159=