Canonical Allele Identifier: CA390751369

Gene: GALC

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87984398A>G , CM000676.2:g.87984398A>G	GRCh38
NC_000014.8:g.88450742A>G , CM000676.1:g.88450742A>G	GRCh37
NC_000014.7:g.87520495A>G	NCBI36
NG_011853.2:g.14166T>C
NG_011853.3:g.14166T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261304.7:c.578T>C MANE Select	ENSP00000261304.2:p.Ile193Thr
ENST00000261304.6:c.578T>C	ENSP00000261304.2:p.Ile193Thr
ENST00000393568.8:c.509T>C	ENSP00000377198.4:p.Ile170Thr
ENST00000393569.6:c.500T>C	ENSP00000377199.2:p.Ile167Thr
ENST00000474294.6:n.568T>C
ENST00000544807.6:c.410T>C	ENSP00000437513.2:p.Ile137Thr
ENST00000554372.5:c.*327T>C	ENSP00000451884.1:n.*327T>C
ENST00000554916.5:n.457T>C
ENST00000556261.5:n.279T>C
ENST00000557316.5:c.578T>C	ENSP00000452314.1:p.Ile193Thr
ENST00000622264.4:c.568T>C
NM_000153.3:c.578T>C	NP_000144.2:p.Ile193Thr
NM_001201401.1:c.509T>C	NP_001188330.1:p.Ile170Thr
NM_001201402.1:c.500T>C	NP_001188331.1:p.Ile167Thr
XM_011536618.1:c.410T>C	XP_011534920.1:p.Ile137Thr
XM_011536618.2:c.410T>C	XP_011534920.1:p.Ile137Thr
NM_000153.4:c.578T>C MANE Select	NP_000144.2:p.Ile193Thr
NM_001201401.2:c.509T>C	NP_001188330.1:p.Ile170Thr
NM_001201402.2:c.500T>C	NP_001188331.1:p.Ile167Thr