Canonical Allele Identifier: CA383030507

Gene: SC5D

Linked Data

• dbSNP Id: rs1947974229
• MyVariant Identifiers: chr11:g.121178045C>T (hg19) ; chr11:g.121307336C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121307336C>T , CM000673.2:g.121307336C>T	GRCh38
NC_000011.9:g.121178045C>T , CM000673.1:g.121178045C>T	GRCh37
NC_000011.8:g.120683255C>T	NCBI36
NG_009446.1:g.19658C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.724C>T MANE Select	ENSP00000264027.4:p.Gln242Ter
ENST00000264027.8:c.724C>T	ENSP00000264027.4:p.Gln242Ter
ENST00000392789.2:c.724C>T	ENSP00000376539.2:p.Gln242Ter
ENST00000527183.1:n.1017C>T
ENST00000534230.5:c.631+93C>T	ENSP00000432550.1:n.631+93C>T
NM_001024956.2:c.724C>T	NP_001020127.1:p.Gln242Ter
NM_006918.4:c.724C>T	NP_008849.2:p.Gln242Ter
NM_006918.5:c.724C>T MANE Select	NP_008849.2:p.Gln242Ter
NM_001024956.3:c.724C>T	NP_001020127.1:p.Gln242Ter