Canonical Allele Identifier: CA2691941357

Gene: SPTAN1

Linked Data

• gnomAD v4: 9-128632368-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632370del , CM000671.2:g.128632370del	GRCh38
NC_000009.11:g.131394649del , CM000671.1:g.131394649del	GRCh37
NC_000009.10:g.130434470del	NCBI36
NG_027748.1:g.84813del
NG_034056.1:g.29482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6995+47del	ENSP00000486547.2:n.6995+47del
ENST00000630866.2:c.7022+47del	ENSP00000487444.1:n.7022+47del
ENST00000704202.1:c.7046+47del	ENSP00000515764.1:n.7046+47del
ENST00000704203.1:c.6995+47del	ENSP00000515765.1:n.6995+47del
ENST00000704204.1:c.6485+47del	ENSP00000515766.1:n.6485+47del
ENST00000704206.1:c.4564+47del
ENST00000704207.1:c.2901+47del
ENST00000706487.1:c.6959+47del	ENSP00000516412.1:n.6959+47del
ENST00000372739.7:c.6959+47del MANE Select	ENSP00000361824.4:n.6959+47del
ENST00000636010.1:n.683+47del
ENST00000358161.9:c.6884+47del	ENSP00000350882.6:n.6884+47del
ENST00000372731.8:c.6944+47del	ENSP00000361816.4:n.6944+47del
ENST00000372739.5:c.6959+47del	ENSP00000361824.3:n.6959+47del
ENST00000625980.2:n.913+47del
ENST00000630763.1:n.716+47del
ENST00000630804.2:c.6899+47del	ENSP00000486308.1:n.6899+47del
ENST00000630866.1:c.7022+47del	ENSP00000487444.1:n.7022+47del
NM_001130438.2:c.6959+47del	NP_001123910.1:n.6959+47del
NM_001195532.1:c.6884+47del	NP_001182461.1:n.6884+47del
NM_003127.3:c.6944+47del	NP_003118.2:n.6944+47del
XM_006717245.1:c.7058+47del	XP_006717308.1:n.7058+47del
XM_006717246.1:c.7043+47del	XP_006717309.1:n.7043+47del
XM_006717247.1:c.6998+47del	XP_006717310.1:n.6998+47del
XM_006717248.1:c.6995+47del	XP_006717311.1:n.6995+47del
XM_006717249.1:c.6980+47del	XP_006717312.1:n.6980+47del
XM_006717250.1:c.6977+47del	XP_006717313.1:n.6977+47del
XM_006717251.1:c.6962+47del	XP_006717314.1:n.6962+47del
XM_006717252.1:c.6935+47del	XP_006717315.1:n.6935+47del
XM_006717253.1:c.6920+47del	XP_006717316.1:n.6920+47del
XM_006717254.1:c.7022+47del	XP_006717317.1:n.7022+47del
NM_001363759.1:c.7022+47del	NP_001350688.1:n.7022+47del
NM_001363765.1:c.6899+47del	NP_001350694.1:n.6899+47del
XM_006717247.2:c.6998+47del	XP_006717310.1:n.6998+47del
XM_006717248.2:c.6995+47del	XP_006717311.1:n.6995+47del
XM_006717251.2:c.6962+47del	XP_006717314.1:n.6962+47del
XM_006717252.3:c.6935+47del	XP_006717315.1:n.6935+47del
XM_017015059.1:c.6941+47del	XP_016870548.1:n.6941+47del
XM_017015060.1:c.6917+47del	XP_016870549.1:n.6917+47del
NM_001130438.3:c.6959+47del MANE Select	NP_001123910.1:n.6959+47del
NM_001195532.2:c.6884+47del	NP_001182461.1:n.6884+47del
NM_001363759.2:c.7022+47del	NP_001350688.1:n.7022+47del
NM_001363765.2:c.6899+47del	NP_001350694.1:n.6899+47del
NM_001375310.1:c.7046+47del	NP_001362239.1:n.7046+47del
NM_001375311.2:c.6959+47del	NP_001362240.1:n.6959+47del
NM_001375312.2:c.6995+47del	NP_001362241.2:n.6995+47del
NM_001375313.1:c.6941+47del	NP_001362242.1:n.6941+47del
NM_001375314.2:c.6899+47del	NP_001362243.1:n.6899+47del
NM_001375318.1:c.7058+47del	NP_001362247.1:n.7058+47del
NM_003127.4:c.6944+47del	NP_003118.2:n.6944+47del