Canonical Allele Identifier: CA2603154228
Gene: SPTAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128617607_128617684dup , CM000671.2:g.128617607_128617684dup GRCh38
NC_000009.11:g.131379886_131379963dup , CM000671.1:g.131379886_131379963dup GRCh37
NC_000009.10:g.130419707_130419784dup NCBI36
NG_027748.1:g.70050_70127dup

Transcript Alleles

HGVS Amino-acid change
ENST00000627441.3:c.5394-33_5438dup
ENST00000630866.2:c.5358-33_5402dup
ENST00000704202.1:c.5358-33_5402dup
ENST00000704203.1:c.5394-33_5438dup
ENST00000704204.1:c.4821-33_4865dup
ENST00000704206.1:c.2981-33_3025dup
ENST00000704207.1:c.968-33_1012dup
ENST00000706487.1:c.5358-33_5402dup
ENST00000372739.7:c.5358-33_5402dup
ENST00000637434.1:n.586-33_630dup
ENST00000358161.9:c.5283-33_5327dup
ENST00000372731.8:c.5343-33_5387dup
ENST00000372739.5:c.5358-33_5402dup
ENST00000630804.2:c.5298-33_5342dup
ENST00000630866.1:c.5358-33_5402dup
NM_001130438.2:c.5358-33_5402dup
NM_001195532.1:c.5283-33_5327dup
NM_003127.3:c.5343-33_5387dup
XM_006717245.1:c.5394-33_5438dup
XM_006717246.1:c.5379-33_5423dup
XM_006717247.1:c.5334-33_5378dup
XM_006717248.1:c.5394-33_5438dup
XM_006717249.1:c.5379-33_5423dup
XM_006717250.1:c.5394-33_5438dup
XM_006717251.1:c.5298-33_5342dup
XM_006717252.1:c.5334-33_5378dup
XM_006717253.1:c.5319-33_5363dup
XM_006717254.1:c.5358-33_5402dup
NM_001363759.1:c.5358-33_5402dup
NM_001363765.1:c.5298-33_5342dup
XM_006717247.2:c.5334-33_5378dup
XM_006717248.2:c.5394-33_5438dup
XM_006717251.2:c.5298-33_5342dup
XM_006717252.3:c.5334-33_5378dup
XM_017015059.1:c.5358-33_5402dup
XM_017015060.1:c.5334-33_5378dup
NM_001130438.3:c.5358-33_5402dup
NM_001195532.2:c.5283-33_5327dup
NM_001363759.2:c.5358-33_5402dup
NM_001363765.2:c.5298-33_5342dup
NM_001375310.1:c.5358-33_5402dup
NM_001375311.2:c.5358-33_5402dup
NM_001375312.2:c.5394-33_5438dup
NM_001375313.1:c.5358-33_5402dup
NM_001375314.2:c.5298-33_5342dup
NM_001375318.1:c.5394-33_5438dup
NM_003127.4:c.5343-33_5387dup