Canonical Allele Identifier: CA1236480

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169733631C>A , CM000663.2:g.169733631C>A	GRCh38
NC_000001.10:g.169702772C>A , CM000663.1:g.169702772C>A	GRCh37
NC_000001.9:g.167969396C>A	NCBI36
NG_012124.1:g.5449G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.-19G>T (SELE) MANE Select	ENSP00000331736.7:n.-19G>T
ENST00000333360.11:c.-19G>T (SELE)	ENSP00000331736.7:n.-19G>T
ENST00000367774.1:c.-19G>T (SELE)	ENSP00000356748.1:n.-19G>T
ENST00000367775.5:c.-19G>T (SELE)	ENSP00000356749.1:n.-19G>T
ENST00000367776.5:c.-19G>T (SELE)	ENSP00000356750.1:n.-19G>T
ENST00000367777.5:c.-19G>T (SELE)	ENSP00000356751.1:n.-19G>T
ENST00000498289.5:n.851+49699C>A (FIRRM)
ENST00000609271.1:c.-19G>T (SELE)	ENSP00000476784.1:n.-19G>T
NM_000450.2:c.-19G>T (SELE) MANE Select	NP_000441.2:n.-19G>T