Canonical Allele Identifier: CA2625961870
Gene: GALC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87984601C>A , CM000676.2:g.87984601C>A GRCh38
NC_000014.8:g.88450945C>A , CM000676.1:g.88450945C>A GRCh37
NC_000014.7:g.87520698C>A NCBI36
NG_011853.2:g.13963G>T
NG_011853.3:g.13963G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.443-68G>T MANE Select ENSP00000261304.2:n.443-68G>T
ENST00000261304.6:c.443-68G>T ENSP00000261304.2:n.443-68G>T
ENST00000393568.8:c.374-68G>T ENSP00000377198.4:n.374-68G>T
ENST00000393569.6:c.365-68G>T ENSP00000377199.2:n.365-68G>T
ENST00000474294.6:n.433-68G>T
ENST00000544807.6:c.275-68G>T ENSP00000437513.2:n.275-68G>T
ENST00000554372.5:c.*192-68G>T ENSP00000451884.1:n.*192-68G>T
ENST00000554916.5:n.322-68G>T
ENST00000556261.5:n.144-68G>T
ENST00000556879.5:c.503-68G>T ENSP00000452208.1:n.503-68G>T
ENST00000557316.5:c.443-68G>T ENSP00000452314.1:n.443-68G>T
ENST00000622264.4:c.433-68G>T
NM_000153.3:c.443-68G>T NP_000144.2:n.443-68G>T
NM_001201401.1:c.374-68G>T NP_001188330.1:n.374-68G>T
NM_001201402.1:c.365-68G>T NP_001188331.1:n.365-68G>T
XM_011536618.1:c.275-68G>T XP_011534920.1:n.275-68G>T
XM_011536618.2:c.275-68G>T XP_011534920.1:n.275-68G>T
NM_000153.4:c.443-68G>T MANE Select NP_000144.2:n.443-68G>T
NM_001201401.2:c.374-68G>T NP_001188330.1:n.374-68G>T
NM_001201402.2:c.365-68G>T NP_001188331.1:n.365-68G>T