Canonical Allele Identifier: CA655657773

Gene: GALC

Linked Data

• COSMIC: COSN20877631

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87934721_87934722insA , CM000676.2:g.87934721_87934722insA	GRCh38
NC_000014.8:g.88401065_88401066insA , CM000676.1:g.88401065_88401066insA	GRCh37
NC_000014.7:g.87470818_87470819insA	NCBI36
NG_011853.2:g.63842_63843insT
NG_011853.3:g.63842_63843insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.*10_*11insT MANE Select	ENSP00000261304.2:n.*10_*11insT
ENST00000261304.6:c.*10_*11insT	ENSP00000261304.2:n.*10_*11insT
ENST00000393568.8:c.*10_*11insT	ENSP00000377198.4:n.*10_*11insT
ENST00000393569.6:c.*10_*11insT	ENSP00000377199.2:n.*10_*11insT
ENST00000544807.6:c.1744-723_1744-722insT	ENSP00000437513.2:n.1744-723_1744-722insT
ENST00000555000.5:c.1279-723_1279-722insT	ENSP00000450472.1:n.1279-723_1279-722insT
NM_000153.3:c.*10_*11insT	NP_000144.2:n.*10_*11insT
NM_001201401.1:c.*10_*11insT	NP_001188330.1:n.*10_*11insT
NM_001201402.1:c.*10_*11insT	NP_001188331.1:n.*10_*11insT
XM_011536618.1:c.*10_*11insT	XP_011534920.1:n.*10_*11insT
XM_011536618.2:c.*10_*11insT	XP_011534920.1:n.*10_*11insT
NM_000153.4:c.*10_*11insT MANE Select	NP_000144.2:n.*10_*11insT
NM_001201401.2:c.*10_*11insT	NP_001188330.1:n.*10_*11insT
NM_001201402.2:c.*10_*11insT	NP_001188331.1:n.*10_*11insT