Canonical Allele Identifier: CA587568359
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1264415148

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648269_34648282del , CM000671.2:g.34648269_34648282del GRCh38
NC_000009.11:g.34648266_34648279del , CM000671.1:g.34648266_34648279del GRCh37
NC_000009.10:g.34638266_34638279del NCBI36
NG_009029.1:g.6632_6645del
NG_028966.1:g.1085_1098del
NG_009029.2:g.6681_6694del

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*153-65_*153-52del ENSP00000509954.1:n.*153-65_*153-52del
ENST00000378842.8:c.565-65_565-52del MANE Select ENSP00000368119.4:n.565-65_565-52del
ENST00000378842.7:c.565-65_565-52del ENSP00000368119.3:n.565-65_565-52del
ENST00000450095.6:c.238-65_238-52del ENSP00000401956.2:n.238-65_238-52del
ENST00000472111.5:n.821-65_821-52del
ENST00000473506.6:c.*153-65_*153-52del ENSP00000432839.2:n.*153-65_*153-52del
ENST00000473529.5:n.724-65_724-52del
ENST00000485531.1:n.1159-65_1159-52del
ENST00000487381.5:n.950-65_950-52del
ENST00000489643.6:n.340-65_340-52del
ENST00000554085.5:c.*309-65_*309-52del ENSP00000450419.1:n.*309-65_*309-52del
ENST00000554139.5:n.811-65_811-52del
ENST00000554550.5:c.*185-65_*185-52del ENSP00000451435.1:n.*185-65_*185-52del
ENST00000554638.5:n.1037-65_1037-52del
ENST00000554897.5:c.*252-65_*252-52del ENSP00000450942.1:n.*252-65_*252-52del
ENST00000554944.5:n.914-65_914-52del
ENST00000555020.5:n.721-65_721-52del
ENST00000555086.5:n.569-65_569-52del
ENST00000555214.5:n.386-65_386-52del
ENST00000556244.1:c.552-65_552-52del
ENST00000556278.1:c.310-65_310-52del ENSP00000451792.1:n.310-65_310-52del
ENST00000556494.5:n.686-65_686-52del
ENST00000557706.5:n.1127-65_1127-52del
NM_000155.3:c.565-65_565-52del NP_000146.2:n.565-65_565-52del
NM_001258332.1:c.238-65_238-52del NP_001245261.1:n.238-65_238-52del
NM_000155.4:c.565-65_565-52del MANE Select NP_000146.2:n.565-65_565-52del
NM_001258332.2:c.238-65_238-52del NP_001245261.1:n.238-65_238-52del