Canonical Allele Identifier: CA375098440

Gene: SPTAN1

Linked Data

• MyVariant Identifiers: chr9:g.131394533A>C (hg19) ; chr9:g.128632254A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128632254A>C , CM000671.2:g.128632254A>C	GRCh38
NC_000009.11:g.131394533A>C , CM000671.1:g.131394533A>C	GRCh37
NC_000009.10:g.130434354A>C	NCBI36
NG_027748.1:g.84697A>C
NG_034056.1:g.29597T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627441.3:c.6926A>C	ENSP00000486547.2:p.Gln2309Pro
ENST00000630866.2:c.6953A>C	ENSP00000487444.1:p.Gln2318Pro
ENST00000704202.1:c.6977A>C	ENSP00000515764.1:p.Gln2326Pro
ENST00000704203.1:c.6926A>C	ENSP00000515765.1:p.Gln2309Pro
ENST00000704204.1:c.6416A>C	ENSP00000515766.1:p.Gln2139Pro
ENST00000704206.1:c.4495A>C
ENST00000704207.1:c.2832A>C
ENST00000706487.1:c.6890A>C	ENSP00000516412.1:p.Gln2297Pro
ENST00000372739.7:c.6890A>C MANE Select	ENSP00000361824.4:p.Gln2297Pro
ENST00000636010.1:n.614A>C
ENST00000358161.9:c.6815A>C	ENSP00000350882.6:p.Gln2272Pro
ENST00000372731.8:c.6875A>C	ENSP00000361816.4:p.Gln2292Pro
ENST00000372739.5:c.6890A>C	ENSP00000361824.3:p.Gln2297Pro
ENST00000625980.2:n.844A>C
ENST00000630763.1:n.647A>C
ENST00000630804.2:c.6830A>C	ENSP00000486308.1:p.Gln2277Pro
ENST00000630866.1:c.6953A>C	ENSP00000487444.1:p.Gln2318Pro
NM_001130438.2:c.6890A>C	NP_001123910.1:p.Gln2297Pro
NM_001195532.1:c.6815A>C	NP_001182461.1:p.Gln2272Pro
NM_003127.3:c.6875A>C	NP_003118.2:p.Gln2292Pro
XM_006717245.1:c.6989A>C	XP_006717308.1:p.Gln2330Pro
XM_006717246.1:c.6974A>C	XP_006717309.1:p.Gln2325Pro
XM_006717247.1:c.6929A>C	XP_006717310.1:p.Gln2310Pro
XM_006717248.1:c.6926A>C	XP_006717311.1:p.Gln2309Pro
XM_006717249.1:c.6911A>C	XP_006717312.1:p.Gln2304Pro
XM_006717250.1:c.6908A>C	XP_006717313.1:p.Gln2303Pro
XM_006717251.1:c.6893A>C	XP_006717314.1:p.Gln2298Pro
XM_006717252.1:c.6866A>C	XP_006717315.1:p.Gln2289Pro
XM_006717253.1:c.6851A>C	XP_006717316.1:p.Gln2284Pro
XM_006717254.1:c.6953A>C	XP_006717317.1:p.Gln2318Pro
NM_001363759.1:c.6953A>C	NP_001350688.1:p.Gln2318Pro
NM_001363765.1:c.6830A>C	NP_001350694.1:p.Gln2277Pro
XM_006717247.2:c.6929A>C	XP_006717310.1:p.Gln2310Pro
XM_006717248.2:c.6926A>C	XP_006717311.1:p.Gln2309Pro
XM_006717251.2:c.6893A>C	XP_006717314.1:p.Gln2298Pro
XM_006717252.3:c.6866A>C	XP_006717315.1:p.Gln2289Pro
XM_017015059.1:c.6872A>C	XP_016870548.1:p.Gln2291Pro
XM_017015060.1:c.6848A>C	XP_016870549.1:p.Gln2283Pro
NM_001130438.3:c.6890A>C MANE Select	NP_001123910.1:p.Gln2297Pro
NM_001195532.2:c.6815A>C	NP_001182461.1:p.Gln2272Pro
NM_001363759.2:c.6953A>C	NP_001350688.1:p.Gln2318Pro
NM_001363765.2:c.6830A>C	NP_001350694.1:p.Gln2277Pro
NM_001375310.1:c.6977A>C	NP_001362239.1:p.Gln2326Pro
NM_001375311.2:c.6890A>C	NP_001362240.1:p.Gln2297Pro
NM_001375312.2:c.6926A>C	NP_001362241.2:p.Gln2309Pro
NM_001375313.1:c.6872A>C	NP_001362242.1:p.Gln2291Pro
NM_001375314.2:c.6830A>C	NP_001362243.1:p.Gln2277Pro
NM_001375318.1:c.6989A>C	NP_001362247.1:p.Gln2330Pro
NM_003127.4:c.6875A>C	NP_003118.2:p.Gln2292Pro