Canonical Allele Identifier: CA259418
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs111033714
MyVariant Identifiers: chr9:g.34648107G>C (hg19) chr9:g.34648110G>C (hg38)
PubMed: PMID:8956044
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648110G>C , CM000671.2:g.34648110G>C GRCh38
NC_000009.11:g.34648107G>C , CM000671.1:g.34648107G>C GRCh37
NC_000009.10:g.34638107G>C NCBI36
NG_009029.1:g.6473G>C
NG_028966.1:g.926G>C
NG_009029.2:g.6522G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*96-5G>C ENSP00000509954.1:n.*96-5G>C
ENST00000378842.8:c.508-5G>C MANE Select ENSP00000368119.4:n.508-5G>C
ENST00000378842.7:c.508-5G>C ENSP00000368119.3:n.508-5G>C
ENST00000450095.6:c.181-5G>C ENSP00000401956.2:n.181-5G>C
ENST00000465543.6:n.847-5G>C
ENST00000472111.5:n.764-5G>C
ENST00000473506.6:c.*96-5G>C ENSP00000432839.2:n.*96-5G>C
ENST00000473529.5:n.662G>C
ENST00000485531.1:n.1097G>C
ENST00000487381.5:n.893-5G>C
ENST00000489643.6:n.283-5G>C
ENST00000554085.5:c.*252-5G>C ENSP00000450419.1:n.*252-5G>C
ENST00000554139.5:n.749G>C
ENST00000554550.5:c.*128-5G>C ENSP00000451435.1:n.*128-5G>C
ENST00000554638.5:n.980-5G>C
ENST00000554897.5:c.*190G>C ENSP00000450942.1:n.*190G>C
ENST00000554944.5:n.852G>C
ENST00000555020.5:n.664-5G>C
ENST00000555086.5:n.512-5G>C
ENST00000555214.5:n.324G>C
ENST00000556244.1:c.495-5G>C
ENST00000556278.1:c.253-5G>C ENSP00000451792.1:n.253-5G>C
ENST00000556494.5:n.629-5G>C
ENST00000557706.5:n.1070-5G>C
NM_000155.3:c.508-5G>C NP_000146.2:n.508-5G>C
NM_001258332.1:c.181-5G>C NP_001245261.1:n.181-5G>C
NM_000155.4:c.508-5G>C MANE Select NP_000146.2:n.508-5G>C
NM_001258332.2:c.181-5G>C NP_001245261.1:n.181-5G>C
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