Canonical Allele Identifier: CA304981457
Gene: CD320 HGNC NCBI
ELAVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8303099_8303101dup , CM000681.2:g.8303099_8303101dup GRCh38
NC_000019.9:g.8367983_8367985dup , CM000681.1:g.8367983_8367985dup GRCh37
NC_000019.8:g.8273983_8273985dup NCBI36
NG_028124.1:g.10257_10259dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301458.10:c.503-120_503-118dup (CD320) MANE Select ENSP00000301458.4:n.503-120_503-118dup
ENST00000301458.9:c.503-120_503-118dup (CD320) ENSP00000301458.4:n.503-120_503-118dup
ENST00000351593.9:c.-87-41096_-87-41094dup (ELAVL1) ENSP00000264073.6:n.-87-41096_-87-41094dup
ENST00000537716.6:c.377-120_377-118dup (CD320) ENSP00000437697.1:n.377-120_377-118dup
ENST00000596002.5:c.*791-120_*791-118dup (CD320) ENSP00000471773.1:n.*791-120_*791-118dup
ENST00000599573.1:c.369-120_369-118dup (CD320)
NM_001165895.1:c.377-120_377-118dup (CD320) NP_001159367.1:n.377-120_377-118dup
NM_016579.3:c.503-120_503-118dup (CD320) NP_057663.1:n.503-120_503-118dup
NM_016579.4:c.503-120_503-118dup (CD320) MANE Select NP_057663.1:n.503-120_503-118dup
NM_001165895.2:c.377-120_377-118dup (CD320) NP_001159367.1:n.377-120_377-118dup