Canonical Allele Identifier: CA375097737

Gene: SPTAN1

Linked Data

• MyVariant Identifiers: chr9:g.131394473T>C (hg19) ; chr9:g.128632194T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632194T>C , CM000671.2:g.128632194T>C	GRCh38
NC_000009.11:g.131394473T>C , CM000671.1:g.131394473T>C	GRCh37
NC_000009.10:g.130434294T>C	NCBI36
NG_027748.1:g.84637T>C
NG_034056.1:g.29657A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6866T>C	ENSP00000486547.2:p.Met2289Thr
ENST00000630866.2:c.6893T>C	ENSP00000487444.1:p.Met2298Thr
ENST00000704202.1:c.6917T>C	ENSP00000515764.1:p.Met2306Thr
ENST00000704203.1:c.6866T>C	ENSP00000515765.1:p.Met2289Thr
ENST00000704204.1:c.6356T>C	ENSP00000515766.1:p.Met2119Thr
ENST00000704206.1:c.4435T>C
ENST00000704207.1:c.2772T>C
ENST00000706487.1:c.6830T>C	ENSP00000516412.1:p.Met2277Thr
ENST00000372739.7:c.6830T>C MANE Select	ENSP00000361824.4:p.Met2277Thr
ENST00000636010.1:n.554T>C
ENST00000358161.9:c.6755T>C	ENSP00000350882.6:p.Met2252Thr
ENST00000372731.8:c.6815T>C	ENSP00000361816.4:p.Met2272Thr
ENST00000372739.5:c.6830T>C	ENSP00000361824.3:p.Met2277Thr
ENST00000625980.2:n.784T>C
ENST00000630763.1:n.587T>C
ENST00000630804.2:c.6770T>C	ENSP00000486308.1:p.Met2257Thr
ENST00000630866.1:c.6893T>C	ENSP00000487444.1:p.Met2298Thr
NM_001130438.2:c.6830T>C	NP_001123910.1:p.Met2277Thr
NM_001195532.1:c.6755T>C	NP_001182461.1:p.Met2252Thr
NM_003127.3:c.6815T>C	NP_003118.2:p.Met2272Thr
XM_006717245.1:c.6929T>C	XP_006717308.1:p.Met2310Thr
XM_006717246.1:c.6914T>C	XP_006717309.1:p.Met2305Thr
XM_006717247.1:c.6869T>C	XP_006717310.1:p.Met2290Thr
XM_006717248.1:c.6866T>C	XP_006717311.1:p.Met2289Thr
XM_006717249.1:c.6851T>C	XP_006717312.1:p.Met2284Thr
XM_006717250.1:c.6848T>C	XP_006717313.1:p.Met2283Thr
XM_006717251.1:c.6833T>C	XP_006717314.1:p.Met2278Thr
XM_006717252.1:c.6806T>C	XP_006717315.1:p.Met2269Thr
XM_006717253.1:c.6791T>C	XP_006717316.1:p.Met2264Thr
XM_006717254.1:c.6893T>C	XP_006717317.1:p.Met2298Thr
NM_001363759.1:c.6893T>C	NP_001350688.1:p.Met2298Thr
NM_001363765.1:c.6770T>C	NP_001350694.1:p.Met2257Thr
XM_006717247.2:c.6869T>C	XP_006717310.1:p.Met2290Thr
XM_006717248.2:c.6866T>C	XP_006717311.1:p.Met2289Thr
XM_006717251.2:c.6833T>C	XP_006717314.1:p.Met2278Thr
XM_006717252.3:c.6806T>C	XP_006717315.1:p.Met2269Thr
XM_017015059.1:c.6812T>C	XP_016870548.1:p.Met2271Thr
XM_017015060.1:c.6788T>C	XP_016870549.1:p.Met2263Thr
NM_001130438.3:c.6830T>C MANE Select	NP_001123910.1:p.Met2277Thr
NM_001195532.2:c.6755T>C	NP_001182461.1:p.Met2252Thr
NM_001363759.2:c.6893T>C	NP_001350688.1:p.Met2298Thr
NM_001363765.2:c.6770T>C	NP_001350694.1:p.Met2257Thr
NM_001375310.1:c.6917T>C	NP_001362239.1:p.Met2306Thr
NM_001375311.2:c.6830T>C	NP_001362240.1:p.Met2277Thr
NM_001375312.2:c.6866T>C	NP_001362241.2:p.Met2289Thr
NM_001375313.1:c.6812T>C	NP_001362242.1:p.Met2271Thr
NM_001375314.2:c.6770T>C	NP_001362243.1:p.Met2257Thr
NM_001375318.1:c.6929T>C	NP_001362247.1:p.Met2310Thr
NM_003127.4:c.6815T>C	NP_003118.2:p.Met2272Thr