Canonical Allele Identifier: CA1880364330

Gene: SPTAN1

Linked Data

• dbSNP Id: rs1857387109
• gnomAD v4: 9-128618020-GACA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128618024_128618026del , CM000671.2:g.128618024_128618026del	GRCh38
NC_000009.11:g.131380303_131380305del , CM000671.1:g.131380303_131380305del	GRCh37
NC_000009.10:g.130420124_130420126del	NCBI36
NG_027748.1:g.70467_70469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.5552_5554del	ENSP00000486547.2:p.Asn1851del
ENST00000630866.2:c.5516_5518del	ENSP00000487444.1:p.Asn1839del
ENST00000704202.1:c.5516_5518del	ENSP00000515764.1:p.Asn1839del
ENST00000704203.1:c.5552_5554del	ENSP00000515765.1:p.Asn1851del
ENST00000704204.1:c.4979_4981del	ENSP00000515766.1:p.Asn1660del
ENST00000704206.1:c.3139_3141del
ENST00000704207.1:c.1126_1128del
ENST00000706487.1:c.5516_5518del	ENSP00000516412.1:p.Asn1839del
ENST00000372739.7:c.5516_5518del MANE Select	ENSP00000361824.4:p.Asn1839del
ENST00000637434.1:n.744_746del
ENST00000358161.9:c.5441_5443del	ENSP00000350882.6:p.Asn1814del
ENST00000372731.8:c.5501_5503del	ENSP00000361816.4:p.Asn1834del
ENST00000372739.5:c.5516_5518del	ENSP00000361824.3:p.Asn1839del
ENST00000630804.2:c.5456_5458del	ENSP00000486308.1:p.Asn1819del
ENST00000630866.1:c.5516_5518del	ENSP00000487444.1:p.Asn1839del
NM_001130438.2:c.5516_5518del	NP_001123910.1:p.Asn1839del
NM_001195532.1:c.5441_5443del	NP_001182461.1:p.Asn1814del
NM_003127.3:c.5501_5503del	NP_003118.2:p.Asn1834del
XM_006717245.1:c.5552_5554del	XP_006717308.1:p.Asn1851del
XM_006717246.1:c.5537_5539del	XP_006717309.1:p.Asn1846del
XM_006717247.1:c.5492_5494del	XP_006717310.1:p.Asn1831del
XM_006717248.1:c.5552_5554del	XP_006717311.1:p.Asn1851del
XM_006717249.1:c.5537_5539del	XP_006717312.1:p.Asn1846del
XM_006717250.1:c.5552_5554del	XP_006717313.1:p.Asn1851del
XM_006717251.1:c.5456_5458del	XP_006717314.1:p.Asn1819del
XM_006717252.1:c.5492_5494del	XP_006717315.1:p.Asn1831del
XM_006717253.1:c.5477_5479del	XP_006717316.1:p.Asn1826del
XM_006717254.1:c.5516_5518del	XP_006717317.1:p.Asn1839del
NM_001363759.1:c.5516_5518del	NP_001350688.1:p.Asn1839del
NM_001363765.1:c.5456_5458del	NP_001350694.1:p.Asn1819del
XM_006717247.2:c.5492_5494del	XP_006717310.1:p.Asn1831del
XM_006717248.2:c.5552_5554del	XP_006717311.1:p.Asn1851del
XM_006717251.2:c.5456_5458del	XP_006717314.1:p.Asn1819del
XM_006717252.3:c.5492_5494del	XP_006717315.1:p.Asn1831del
XM_017015059.1:c.5516_5518del	XP_016870548.1:p.Asn1839del
XM_017015060.1:c.5492_5494del	XP_016870549.1:p.Asn1831del
NM_001130438.3:c.5516_5518del MANE Select	NP_001123910.1:p.Asn1839del
NM_001195532.2:c.5441_5443del	NP_001182461.1:p.Asn1814del
NM_001363759.2:c.5516_5518del	NP_001350688.1:p.Asn1839del
NM_001363765.2:c.5456_5458del	NP_001350694.1:p.Asn1819del
NM_001375310.1:c.5516_5518del	NP_001362239.1:p.Asn1839del
NM_001375311.2:c.5516_5518del	NP_001362240.1:p.Asn1839del
NM_001375312.2:c.5552_5554del	NP_001362241.2:p.Asn1851del
NM_001375313.1:c.5516_5518del	NP_001362242.1:p.Asn1839del
NM_001375314.2:c.5456_5458del	NP_001362243.1:p.Asn1819del
NM_001375318.1:c.5552_5554del	NP_001362247.1:p.Asn1851del
NM_003127.4:c.5501_5503del	NP_003118.2:p.Asn1834del