Canonical Allele Identifier: CA2689808731
Gene: GALT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648326_34648327insA , CM000671.2:g.34648326_34648327insA GRCh38
NC_000009.11:g.34648323_34648324insA , CM000671.1:g.34648323_34648324insA GRCh37
NC_000009.10:g.34638323_34638324insA NCBI36
NG_009029.1:g.6689_6690insA
NG_028966.1:g.1142_1143insA
NG_009029.2:g.6738_6739insA

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*153-8_*153-7insA ENSP00000509954.1:n.*153-8_*153-7insA
ENST00000378842.8:c.565-8_565-7insA MANE Select ENSP00000368119.4:n.565-8_565-7insA
ENST00000378842.7:c.565-8_565-7insA ENSP00000368119.3:n.565-8_565-7insA
ENST00000450095.6:c.238-8_238-7insA ENSP00000401956.2:n.238-8_238-7insA
ENST00000472111.5:n.821-8_821-7insA
ENST00000473506.6:c.*153-8_*153-7insA ENSP00000432839.2:n.*153-8_*153-7insA
ENST00000473529.5:n.724-8_724-7insA
ENST00000485531.1:n.1159-8_1159-7insA
ENST00000487381.5:n.950-8_950-7insA
ENST00000489643.6:n.340-8_340-7insA
ENST00000554085.5:c.*309-8_*309-7insA ENSP00000450419.1:n.*309-8_*309-7insA
ENST00000554139.5:n.811-8_811-7insA
ENST00000554550.5:c.*185-8_*185-7insA ENSP00000451435.1:n.*185-8_*185-7insA
ENST00000554638.5:n.1037-8_1037-7insA
ENST00000554897.5:c.*252-8_*252-7insA ENSP00000450942.1:n.*252-8_*252-7insA
ENST00000554944.5:n.914-8_914-7insA
ENST00000555020.5:n.721-8_721-7insA
ENST00000555086.5:n.569-8_569-7insA
ENST00000555214.5:n.386-8_386-7insA
ENST00000556244.1:c.552-8_552-7insA
ENST00000556278.1:c.310-8_310-7insA ENSP00000451792.1:n.310-8_310-7insA
ENST00000556494.5:n.686-8_686-7insA
ENST00000557706.5:n.1127-8_1127-7insA
NM_000155.3:c.565-8_565-7insA NP_000146.2:n.565-8_565-7insA
NM_001258332.1:c.238-8_238-7insA NP_001245261.1:n.238-8_238-7insA
NM_000155.4:c.565-8_565-7insA MANE Select NP_000146.2:n.565-8_565-7insA
NM_001258332.2:c.238-8_238-7insA NP_001245261.1:n.238-8_238-7insA