Canonical Allele Identifier: CA655657768

Gene: GALC

Linked Data

• COSMIC: COSN20078058

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934680_87934681insG , CM000676.2:g.87934680_87934681insG	GRCh38
NC_000014.8:g.88401024_88401025insG , CM000676.1:g.88401024_88401025insG	GRCh37
NC_000014.7:g.87470777_87470778insG	NCBI36
NG_011853.2:g.63883_63884insC
NG_011853.3:g.63883_63884insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.*51_*52insC MANE Select	ENSP00000261304.2:n.*51_*52insC
ENST00000261304.6:c.*51_*52insC	ENSP00000261304.2:n.*51_*52insC
ENST00000393569.6:c.*51_*52insC	ENSP00000377199.2:n.*51_*52insC
ENST00000544807.6:c.1744-682_1744-681insC	ENSP00000437513.2:n.1744-682_1744-681insC
ENST00000555000.5:c.1279-682_1279-681insC	ENSP00000450472.1:n.1279-682_1279-681insC
NM_000153.3:c.*51_*52insC	NP_000144.2:n.*51_*52insC
NM_001201401.1:c.*51_*52insC	NP_001188330.1:n.*51_*52insC
NM_001201402.1:c.*51_*52insC	NP_001188331.1:n.*51_*52insC
XM_011536618.1:c.*51_*52insC	XP_011534920.1:n.*51_*52insC
XM_011536618.2:c.*51_*52insC	XP_011534920.1:n.*51_*52insC
NM_000153.4:c.*51_*52insC MANE Select	NP_000144.2:n.*51_*52insC
NM_001201401.2:c.*51_*52insC	NP_001188330.1:n.*51_*52insC
NM_001201402.2:c.*51_*52insC	NP_001188331.1:n.*51_*52insC