Canonical Allele Identifier: CA383029981
Gene: SC5D HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.121177938T>C (hg19) chr11:g.121307229T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121307229T>C , CM000673.2:g.121307229T>C GRCh38
NC_000011.9:g.121177938T>C , CM000673.1:g.121177938T>C GRCh37
NC_000011.8:g.120683148T>C NCBI36
NG_009446.1:g.19551T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264027.9:c.617T>C MANE Select ENSP00000264027.4:p.Ile206Thr
ENST00000264027.8:c.617T>C ENSP00000264027.4:p.Ile206Thr
ENST00000392789.2:c.617T>C ENSP00000376539.2:p.Ile206Thr
ENST00000527183.1:n.910T>C
ENST00000528991.1:n.310T>C
ENST00000534230.5:c.617T>C ENSP00000432550.1:p.Ile206Thr
NM_001024956.2:c.617T>C NP_001020127.1:p.Ile206Thr
NM_006918.4:c.617T>C NP_008849.2:p.Ile206Thr
NM_006918.5:c.617T>C MANE Select NP_008849.2:p.Ile206Thr
NM_001024956.3:c.617T>C NP_001020127.1:p.Ile206Thr
Search 100 bp 5'
Search 100 bp 3'