Canonical Allele Identifier: CA890964319

Gene: SELE FIRRM

Linked Data

• dbSNP Id: rs1281215041
• MyVariant Identifiers: chr1:g.169700919A>G (hg19) ; chr1:g.169731778A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731778A>G , CM000663.2:g.169731778A>G	GRCh38
NC_000001.10:g.169700919A>G , CM000663.1:g.169700919A>G	GRCh37
NC_000001.9:g.167967543A>G	NCBI36
NG_012124.1:g.7302T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.529+57T>C (SELE) MANE Select	ENSP00000331736.7:n.529+57T>C
ENST00000333360.11:c.529+57T>C (SELE)	ENSP00000331736.7:n.529+57T>C
ENST00000367774.1:c.529+57T>C (SELE)	ENSP00000356748.1:n.529+57T>C
ENST00000367775.5:c.529+57T>C (SELE)	ENSP00000356749.1:n.529+57T>C
ENST00000367776.5:c.529+57T>C (SELE)	ENSP00000356750.1:n.529+57T>C
ENST00000367777.5:c.529+57T>C (SELE)	ENSP00000356751.1:n.529+57T>C
ENST00000461085.1:n.269T>C (SELE)
ENST00000498289.5:n.851+47846A>G (FIRRM)
NM_000450.2:c.529+57T>C (SELE) MANE Select	NP_000441.2:n.529+57T>C