Canonical Allele Identifier: CA375097747

Gene: SPTAN1

Linked Data

• MyVariant Identifiers: chr9:g.131394474G>C (hg19) ; chr9:g.128632195G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632195G>C , CM000671.2:g.128632195G>C	GRCh38
NC_000009.11:g.131394474G>C , CM000671.1:g.131394474G>C	GRCh37
NC_000009.10:g.130434295G>C	NCBI36
NG_027748.1:g.84638G>C
NG_034056.1:g.29656C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6867G>C	ENSP00000486547.2:p.Met2289Ile
ENST00000630866.2:c.6894G>C	ENSP00000487444.1:p.Met2298Ile
ENST00000704202.1:c.6918G>C	ENSP00000515764.1:p.Met2306Ile
ENST00000704203.1:c.6867G>C	ENSP00000515765.1:p.Met2289Ile
ENST00000704204.1:c.6357G>C	ENSP00000515766.1:p.Met2119Ile
ENST00000704206.1:c.4436G>C
ENST00000704207.1:c.2773G>C
ENST00000706487.1:c.6831G>C	ENSP00000516412.1:p.Met2277Ile
ENST00000372739.7:c.6831G>C MANE Select	ENSP00000361824.4:p.Met2277Ile
ENST00000636010.1:n.555G>C
ENST00000358161.9:c.6756G>C	ENSP00000350882.6:p.Met2252Ile
ENST00000372731.8:c.6816G>C	ENSP00000361816.4:p.Met2272Ile
ENST00000372739.5:c.6831G>C	ENSP00000361824.3:p.Met2277Ile
ENST00000625980.2:n.785G>C
ENST00000630763.1:n.588G>C
ENST00000630804.2:c.6771G>C	ENSP00000486308.1:p.Met2257Ile
ENST00000630866.1:c.6894G>C	ENSP00000487444.1:p.Met2298Ile
NM_001130438.2:c.6831G>C	NP_001123910.1:p.Met2277Ile
NM_001195532.1:c.6756G>C	NP_001182461.1:p.Met2252Ile
NM_003127.3:c.6816G>C	NP_003118.2:p.Met2272Ile
XM_006717245.1:c.6930G>C	XP_006717308.1:p.Met2310Ile
XM_006717246.1:c.6915G>C	XP_006717309.1:p.Met2305Ile
XM_006717247.1:c.6870G>C	XP_006717310.1:p.Met2290Ile
XM_006717248.1:c.6867G>C	XP_006717311.1:p.Met2289Ile
XM_006717249.1:c.6852G>C	XP_006717312.1:p.Met2284Ile
XM_006717250.1:c.6849G>C	XP_006717313.1:p.Met2283Ile
XM_006717251.1:c.6834G>C	XP_006717314.1:p.Met2278Ile
XM_006717252.1:c.6807G>C	XP_006717315.1:p.Met2269Ile
XM_006717253.1:c.6792G>C	XP_006717316.1:p.Met2264Ile
XM_006717254.1:c.6894G>C	XP_006717317.1:p.Met2298Ile
NM_001363759.1:c.6894G>C	NP_001350688.1:p.Met2298Ile
NM_001363765.1:c.6771G>C	NP_001350694.1:p.Met2257Ile
XM_006717247.2:c.6870G>C	XP_006717310.1:p.Met2290Ile
XM_006717248.2:c.6867G>C	XP_006717311.1:p.Met2289Ile
XM_006717251.2:c.6834G>C	XP_006717314.1:p.Met2278Ile
XM_006717252.3:c.6807G>C	XP_006717315.1:p.Met2269Ile
XM_017015059.1:c.6813G>C	XP_016870548.1:p.Met2271Ile
XM_017015060.1:c.6789G>C	XP_016870549.1:p.Met2263Ile
NM_001130438.3:c.6831G>C MANE Select	NP_001123910.1:p.Met2277Ile
NM_001195532.2:c.6756G>C	NP_001182461.1:p.Met2252Ile
NM_001363759.2:c.6894G>C	NP_001350688.1:p.Met2298Ile
NM_001363765.2:c.6771G>C	NP_001350694.1:p.Met2257Ile
NM_001375310.1:c.6918G>C	NP_001362239.1:p.Met2306Ile
NM_001375311.2:c.6831G>C	NP_001362240.1:p.Met2277Ile
NM_001375312.2:c.6867G>C	NP_001362241.2:p.Met2289Ile
NM_001375313.1:c.6813G>C	NP_001362242.1:p.Met2271Ile
NM_001375314.2:c.6771G>C	NP_001362243.1:p.Met2257Ile
NM_001375318.1:c.6930G>C	NP_001362247.1:p.Met2310Ile
NM_003127.4:c.6816G>C	NP_003118.2:p.Met2272Ile