Canonical Allele Identifier: CA2153352627
Gene: GALC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87939790_87939792delinsCTT , CM000676.2:g.87939790_87939792delinsCTT GRCh38
NC_000014.8:g.88406134_88406136delinsCTT , CM000676.1:g.88406134_88406136delinsCTT GRCh37
NC_000014.7:g.87475887_87475889delinsCTT NCBI36
NG_011853.2:g.58772_58774delinsAAG
NG_011853.3:g.58772_58774delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000261304.7:c.1911+113_1911+115delinsAAG MANE Select ENSP00000261304.2:n.1911+113_1911+115delinsAAG
ENST00000261304.6:c.1911+113_1911+115delinsAAG ENSP00000261304.2:n.1911+113_1911+115delinsAAG
ENST00000393568.8:c.1842+113_1842+115delinsAAG ENSP00000377198.4:n.1842+113_1842+115delinsAAG
ENST00000393569.6:c.1833+113_1833+115delinsAAG ENSP00000377199.2:n.1833+113_1833+115delinsAAG
ENST00000544807.6:c.1743+113_1743+115delinsAAG ENSP00000437513.2:n.1743+113_1743+115delinsAAG
ENST00000555000.5:c.1278+113_1278+115delinsAAG ENSP00000450472.1:n.1278+113_1278+115delinsAAG
ENST00000555179.1:c.447+113_447+115delinsAAG
NM_000153.3:c.1911+113_1911+115delinsAAG NP_000144.2:n.1911+113_1911+115delinsAAG
NM_001201401.1:c.1842+113_1842+115delinsAAG NP_001188330.1:n.1842+113_1842+115delinsAAG
NM_001201402.1:c.1833+113_1833+115delinsAAG NP_001188331.1:n.1833+113_1833+115delinsAAG
XM_011536618.1:c.1743+113_1743+115delinsAAG XP_011534920.1:n.1743+113_1743+115delinsAAG
XM_011536618.2:c.1743+113_1743+115delinsAAG XP_011534920.1:n.1743+113_1743+115delinsAAG
NM_000153.4:c.1911+113_1911+115delinsAAG MANE Select NP_000144.2:n.1911+113_1911+115delinsAAG
NM_001201401.2:c.1842+113_1842+115delinsAAG NP_001188330.1:n.1842+113_1842+115delinsAAG
NM_001201402.2:c.1833+113_1833+115delinsAAG NP_001188331.1:n.1833+113_1833+115delinsAAG