Canonical Allele Identifier: CA421740764

Gene: SELE FIRRM

Linked Data

• dbSNP Id: rs1648918680
• MyVariant Identifiers: chr1:g.169700983A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731842A>G , CM000663.2:g.169731842A>G	GRCh38
NC_000001.10:g.169700983A>G , CM000663.1:g.169700983A>G	GRCh37
NC_000001.9:g.167967607A>G	NCBI36
NG_012124.1:g.7238T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.522T>C (SELE) MANE Select	ENSP00000331736.7:p.Cys174=
ENST00000333360.11:c.522T>C (SELE)	ENSP00000331736.7:p.Cys174=
ENST00000367774.1:c.522T>C (SELE)	ENSP00000356748.1:p.Cys174=
ENST00000367775.5:c.522T>C (SELE)	ENSP00000356749.1:p.Cys174=
ENST00000367776.5:c.522T>C (SELE)	ENSP00000356750.1:p.Cys174=
ENST00000367777.5:c.522T>C (SELE)	ENSP00000356751.1:p.Cys174=
ENST00000461085.1:n.205T>C (SELE)
ENST00000498289.5:n.851+47910A>G (FIRRM)
NM_000450.2:c.522T>C (SELE) MANE Select	NP_000441.2:p.Cys174=