Canonical Allele Identifier: CA373279118

Gene: GALT

Linked Data

• ClinVar Variation Id: 2675829
• ClinVar RCV Id: RCV003461647
• gnomAD v4: 9-34647506-C-G
• MyVariant Identifiers: chr9:g.34647503C>G (hg19) ; chr9:g.34647506C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647506C>G , CM000671.2:g.34647506C>G	GRCh38
NC_000009.11:g.34647503C>G , CM000671.1:g.34647503C>G	GRCh37
NC_000009.10:g.34637503C>G	NCBI36
NG_009029.1:g.5869C>G
NG_028966.1:g.322C>G
NG_009029.2:g.5918C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.267C>G	ENSP00000509954.1:p.Tyr89Ter
ENST00000378842.8:c.267C>G MANE Select	ENSP00000368119.4:p.Tyr89Ter
ENST00000378842.7:c.267C>G	ENSP00000368119.3:p.Tyr89Ter
ENST00000450095.6:c.50+248C>G	ENSP00000401956.2:n.50+248C>G
ENST00000465543.6:n.606C>G
ENST00000468099.2:n.540C>G
ENST00000472111.5:n.308C>G
ENST00000473506.6:c.253-35C>G	ENSP00000432839.2:n.253-35C>G
ENST00000473529.5:n.314C>G
ENST00000485531.1:n.493C>G
ENST00000487381.5:n.526C>G
ENST00000489643.6:n.282+248C>G
ENST00000554085.5:c.*11C>G	ENSP00000450419.1:n.*11C>G
ENST00000554139.5:n.320C>G
ENST00000554330.5:n.250-35C>G
ENST00000554550.5:c.252+248C>G	ENSP00000451435.1:n.252+248C>G
ENST00000554638.5:n.524C>G
ENST00000554897.5:c.252+248C>G	ENSP00000450942.1:n.252+248C>G
ENST00000554944.5:n.283-35C>G
ENST00000555020.5:n.297C>G
ENST00000555086.5:n.271C>G
ENST00000555214.5:n.261+248C>G
ENST00000556157.1:n.391C>G
ENST00000556244.1:c.254C>G
ENST00000556278.1:c.252+248C>G	ENSP00000451792.1:n.252+248C>G
ENST00000556403.5:n.280C>G
ENST00000556494.5:n.299C>G
ENST00000557541.5:n.446-35C>G
ENST00000557706.5:n.614C>G
NM_000155.3:c.267C>G	NP_000146.2:p.Tyr89Ter
NM_001258332.1:c.50+248C>G	NP_001245261.1:n.50+248C>G
NM_000155.4:c.267C>G MANE Select	NP_000146.2:p.Tyr89Ter
NM_001258332.2:c.50+248C>G	NP_001245261.1:n.50+248C>G