Canonical Allele Identifier: CA373280656

Gene: GALT

Linked Data

• gnomAD v4: 9-34647858-C-A
• MyVariant Identifiers: chr9:g.34647855C>A (hg19) ; chr9:g.34647858C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647858C>A , CM000671.2:g.34647858C>A	GRCh38
NC_000009.11:g.34647855C>A , CM000671.1:g.34647855C>A	GRCh37
NC_000009.10:g.34637855C>A	NCBI36
NG_009029.1:g.6221C>A
NG_028966.1:g.674C>A
NG_009029.2:g.6270C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.355C>A	ENSP00000509954.1:p.Arg119=
ENST00000378842.8:c.404C>A MANE Select	ENSP00000368119.4:p.Ser135Ter
ENST00000378842.7:c.404C>A	ENSP00000368119.3:p.Ser135Ter
ENST00000450095.6:c.77C>A	ENSP00000401956.2:p.Ser26Ter
ENST00000465543.6:n.743C>A
ENST00000472111.5:n.660C>A
ENST00000473506.6:c.355C>A	ENSP00000432839.2:p.Arg119=
ENST00000473529.5:n.540C>A
ENST00000485531.1:n.845C>A
ENST00000487381.5:n.789C>A
ENST00000489643.6:n.283-257C>A
ENST00000554085.5:c.*148C>A	ENSP00000450419.1:n.*148C>A
ENST00000554139.5:n.583C>A
ENST00000554550.5:c.*24C>A	ENSP00000451435.1:n.*24C>A
ENST00000554638.5:n.876C>A
ENST00000554897.5:c.*24C>A	ENSP00000450942.1:n.*24C>A
ENST00000554944.5:n.600C>A
ENST00000555020.5:n.560C>A
ENST00000555086.5:n.408C>A
ENST00000555214.5:n.262-190C>A
ENST00000556244.1:c.391C>A
ENST00000556278.1:c.253-257C>A	ENSP00000451792.1:n.253-257C>A
ENST00000556494.5:n.525C>A
ENST00000557541.5:n.548C>A
ENST00000557706.5:n.966C>A
NM_000155.3:c.404C>A	NP_000146.2:p.Ser135Ter
NM_001258332.1:c.77C>A	NP_001245261.1:p.Ser26Ter
NM_000155.4:c.404C>A MANE Select	NP_000146.2:p.Ser135Ter
NM_001258332.2:c.77C>A	NP_001245261.1:p.Ser26Ter