Canonical Allele Identifier: CA2689808602

Gene: GALT

Linked Data

• gnomAD v4: 9-34647407-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647407C>G , CM000671.2:g.34647407C>G	GRCh38
NC_000009.11:g.34647404C>G , CM000671.1:g.34647404C>G	GRCh37
NC_000009.10:g.34637404C>G	NCBI36
NG_009029.1:g.5770C>G
NG_028966.1:g.223C>G
NG_009029.2:g.5819C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.253-85C>G	ENSP00000509954.1:n.253-85C>G
ENST00000378842.8:c.253-85C>G MANE Select	ENSP00000368119.4:n.253-85C>G
ENST00000378842.7:c.253-85C>G	ENSP00000368119.3:n.253-85C>G
ENST00000450095.6:c.50+149C>G	ENSP00000401956.2:n.50+149C>G
ENST00000465543.6:n.592-85C>G
ENST00000468099.2:n.441C>G
ENST00000472111.5:n.294-85C>G
ENST00000473506.6:c.253-134C>G	ENSP00000432839.2:n.253-134C>G
ENST00000473529.5:n.300-85C>G
ENST00000485531.1:n.394C>G
ENST00000487381.5:n.427C>G
ENST00000489643.6:n.282+149C>G
ENST00000554085.5:c.253-68C>G	ENSP00000450419.1:n.253-68C>G
ENST00000554139.5:n.306-85C>G
ENST00000554330.5:n.250-134C>G
ENST00000554550.5:c.252+149C>G	ENSP00000451435.1:n.252+149C>G
ENST00000554638.5:n.425C>G
ENST00000554897.5:c.252+149C>G	ENSP00000450942.1:n.252+149C>G
ENST00000554944.5:n.283-134C>G
ENST00000555020.5:n.283-85C>G
ENST00000555086.5:n.257-85C>G
ENST00000555214.5:n.261+149C>G
ENST00000556157.1:n.360-68C>G
ENST00000556244.1:c.155C>G
ENST00000556278.1:c.252+149C>G	ENSP00000451792.1:n.252+149C>G
ENST00000556403.5:n.266-85C>G
ENST00000556494.5:n.285-85C>G
ENST00000557541.5:n.446-134C>G
ENST00000557706.5:n.515C>G
NM_000155.3:c.253-85C>G	NP_000146.2:n.253-85C>G
NM_001258332.1:c.50+149C>G	NP_001245261.1:n.50+149C>G
NM_000155.4:c.253-85C>G MANE Select	NP_000146.2:n.253-85C>G
NM_001258332.2:c.50+149C>G	NP_001245261.1:n.50+149C>G