Canonical Allele Identifier: CA467304834

Gene: SPTAN1

Linked Data

• MyVariant Identifiers: chr9:g.131394513C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632234C>T , CM000671.2:g.128632234C>T	GRCh38
NC_000009.11:g.131394513C>T , CM000671.1:g.131394513C>T	GRCh37
NC_000009.10:g.130434334C>T	NCBI36
NG_027748.1:g.84677C>T
NG_034056.1:g.29617G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6906C>T	ENSP00000486547.2:p.His2302=
ENST00000630866.2:c.6933C>T	ENSP00000487444.1:p.His2311=
ENST00000704202.1:c.6957C>T	ENSP00000515764.1:p.His2319=
ENST00000704203.1:c.6906C>T	ENSP00000515765.1:p.His2302=
ENST00000704204.1:c.6396C>T	ENSP00000515766.1:p.His2132=
ENST00000704206.1:c.4475C>T
ENST00000704207.1:c.2812C>T
ENST00000706487.1:c.6870C>T	ENSP00000516412.1:p.His2290=
ENST00000372739.7:c.6870C>T MANE Select	ENSP00000361824.4:p.His2290=
ENST00000636010.1:n.594C>T
ENST00000358161.9:c.6795C>T	ENSP00000350882.6:p.His2265=
ENST00000372731.8:c.6855C>T	ENSP00000361816.4:p.His2285=
ENST00000372739.5:c.6870C>T	ENSP00000361824.3:p.His2290=
ENST00000625980.2:n.824C>T
ENST00000630763.1:n.627C>T
ENST00000630804.2:c.6810C>T	ENSP00000486308.1:p.His2270=
ENST00000630866.1:c.6933C>T	ENSP00000487444.1:p.His2311=
NM_001130438.2:c.6870C>T	NP_001123910.1:p.His2290=
NM_001195532.1:c.6795C>T	NP_001182461.1:p.His2265=
NM_003127.3:c.6855C>T	NP_003118.2:p.His2285=
XM_006717245.1:c.6969C>T	XP_006717308.1:p.His2323=
XM_006717246.1:c.6954C>T	XP_006717309.1:p.His2318=
XM_006717247.1:c.6909C>T	XP_006717310.1:p.His2303=
XM_006717248.1:c.6906C>T	XP_006717311.1:p.His2302=
XM_006717249.1:c.6891C>T	XP_006717312.1:p.His2297=
XM_006717250.1:c.6888C>T	XP_006717313.1:p.His2296=
XM_006717251.1:c.6873C>T	XP_006717314.1:p.His2291=
XM_006717252.1:c.6846C>T	XP_006717315.1:p.His2282=
XM_006717253.1:c.6831C>T	XP_006717316.1:p.His2277=
XM_006717254.1:c.6933C>T	XP_006717317.1:p.His2311=
NM_001363759.1:c.6933C>T	NP_001350688.1:p.His2311=
NM_001363765.1:c.6810C>T	NP_001350694.1:p.His2270=
XM_006717247.2:c.6909C>T	XP_006717310.1:p.His2303=
XM_006717248.2:c.6906C>T	XP_006717311.1:p.His2302=
XM_006717251.2:c.6873C>T	XP_006717314.1:p.His2291=
XM_006717252.3:c.6846C>T	XP_006717315.1:p.His2282=
XM_017015059.1:c.6852C>T	XP_016870548.1:p.His2284=
XM_017015060.1:c.6828C>T	XP_016870549.1:p.His2276=
NM_001130438.3:c.6870C>T MANE Select	NP_001123910.1:p.His2290=
NM_001195532.2:c.6795C>T	NP_001182461.1:p.His2265=
NM_001363759.2:c.6933C>T	NP_001350688.1:p.His2311=
NM_001363765.2:c.6810C>T	NP_001350694.1:p.His2270=
NM_001375310.1:c.6957C>T	NP_001362239.1:p.His2319=
NM_001375311.2:c.6870C>T	NP_001362240.1:p.His2290=
NM_001375312.2:c.6906C>T	NP_001362241.2:p.His2302=
NM_001375313.1:c.6852C>T	NP_001362242.1:p.His2284=
NM_001375314.2:c.6810C>T	NP_001362243.1:p.His2270=
NM_001375318.1:c.6969C>T	NP_001362247.1:p.His2323=
NM_003127.4:c.6855C>T	NP_003118.2:p.His2285=