Canonical Allele Identifier: CA2625980970
Gene: GALC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.87988328T>A , CM000676.2:g.87988328T>A GRCh38
NC_000014.8:g.88454672T>A , CM000676.1:g.88454672T>A GRCh37
NC_000014.7:g.87524425T>A NCBI36
NG_011853.2:g.10236A>T
NG_011853.3:g.10236A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261304.7:c.265-121A>T MANE Select ENSP00000261304.2:n.265-121A>T
ENST00000261304.6:c.265-121A>T ENSP00000261304.2:n.265-121A>T
ENST00000393568.8:c.196-121A>T ENSP00000377198.4:n.196-121A>T
ENST00000393569.6:c.187-121A>T ENSP00000377199.2:n.187-121A>T
ENST00000474294.6:n.255-121A>T
ENST00000544807.6:c.97-121A>T ENSP00000437513.2:n.97-121A>T
ENST00000554372.5:c.265-121A>T ENSP00000451884.1:n.265-121A>T
ENST00000554916.5:n.144-121A>T
ENST00000555956.1:n.70-121A>T
ENST00000556879.5:c.325-121A>T ENSP00000452208.1:n.325-121A>T
ENST00000557316.5:c.265-121A>T ENSP00000452314.1:n.265-121A>T
ENST00000622264.4:c.255-121A>T
NM_000153.3:c.265-121A>T NP_000144.2:n.265-121A>T
NM_001201401.1:c.196-121A>T NP_001188330.1:n.196-121A>T
NM_001201402.1:c.187-121A>T NP_001188331.1:n.187-121A>T
XM_011536618.1:c.97-121A>T XP_011534920.1:n.97-121A>T
XM_011536618.2:c.97-121A>T XP_011534920.1:n.97-121A>T
NM_000153.4:c.265-121A>T MANE Select NP_000144.2:n.265-121A>T
NM_001201401.2:c.196-121A>T NP_001188330.1:n.196-121A>T
NM_001201402.2:c.187-121A>T NP_001188331.1:n.187-121A>T