Canonical Allele Identifier: CA884272566

Gene: CD320 ELAVL1

Linked Data

• dbSNP Id: rs1463561714
• MyVariant Identifiers: chr19:g.8369837C>A (hg19) ; chr19:g.8304953C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8304953C>A , CM000681.2:g.8304953C>A	GRCh38
NC_000019.9:g.8369837C>A , CM000681.1:g.8369837C>A	GRCh37
NC_000019.8:g.8275837C>A	NCBI36
NG_028124.1:g.8404G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000301458.10:c.268+78G>T (CD320) MANE Select	ENSP00000301458.4:n.268+78G>T
ENST00000301458.9:c.268+78G>T (CD320)	ENSP00000301458.4:n.268+78G>T
ENST00000351593.9:c.-87-42949G>T (ELAVL1)	ENSP00000264073.6:n.-87-42949G>T
ENST00000537716.6:c.143-865G>T (CD320)	ENSP00000437697.1:n.143-865G>T
ENST00000596002.5:c.*671+78G>T (CD320)	ENSP00000471773.1:n.*671+78G>T
ENST00000598299.1:n.391G>T (CD320)
ENST00000599573.1:c.249+78G>T (CD320)
NM_001165895.1:c.143-865G>T (CD320)	NP_001159367.1:n.143-865G>T
NM_016579.3:c.268+78G>T (CD320)	NP_057663.1:n.268+78G>T
NM_016579.4:c.268+78G>T (CD320) MANE Select	NP_057663.1:n.268+78G>T
NM_001165895.2:c.143-865G>T (CD320)	NP_001159367.1:n.143-865G>T