Canonical Allele Identifier: CA1845638423
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821160769

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648290G>A , CM000671.2:g.34648290G>A GRCh38
NC_000009.11:g.34648287G>A , CM000671.1:g.34648287G>A GRCh37
NC_000009.10:g.34638287G>A NCBI36
NG_009029.1:g.6653G>A
NG_028966.1:g.1106G>A
NG_009029.2:g.6702G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*153-44G>A ENSP00000509954.1:n.*153-44G>A
ENST00000378842.8:c.565-44G>A MANE Select ENSP00000368119.4:n.565-44G>A
ENST00000378842.7:c.565-44G>A ENSP00000368119.3:n.565-44G>A
ENST00000450095.6:c.238-44G>A ENSP00000401956.2:n.238-44G>A
ENST00000472111.5:n.821-44G>A
ENST00000473506.6:c.*153-44G>A ENSP00000432839.2:n.*153-44G>A
ENST00000473529.5:n.724-44G>A
ENST00000485531.1:n.1159-44G>A
ENST00000487381.5:n.950-44G>A
ENST00000489643.6:n.340-44G>A
ENST00000554085.5:c.*309-44G>A ENSP00000450419.1:n.*309-44G>A
ENST00000554139.5:n.811-44G>A
ENST00000554550.5:c.*185-44G>A ENSP00000451435.1:n.*185-44G>A
ENST00000554638.5:n.1037-44G>A
ENST00000554897.5:c.*252-44G>A ENSP00000450942.1:n.*252-44G>A
ENST00000554944.5:n.914-44G>A
ENST00000555020.5:n.721-44G>A
ENST00000555086.5:n.569-44G>A
ENST00000555214.5:n.386-44G>A
ENST00000556244.1:c.552-44G>A
ENST00000556278.1:c.310-44G>A ENSP00000451792.1:n.310-44G>A
ENST00000556494.5:n.686-44G>A
ENST00000557706.5:n.1127-44G>A
NM_000155.3:c.565-44G>A NP_000146.2:n.565-44G>A
NM_001258332.1:c.238-44G>A NP_001245261.1:n.238-44G>A
NM_000155.4:c.565-44G>A MANE Select NP_000146.2:n.565-44G>A
NM_001258332.2:c.238-44G>A NP_001245261.1:n.238-44G>A