Canonical Allele Identifier: CA350708799

Gene: SPEG ASIC4-AS1

Linked Data

• MyVariant Identifiers: chr2:g.220353911C>A (hg19) ; chr2:g.219489189C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489189C>A , CM000664.2:g.219489189C>A	GRCh38
NC_000002.11:g.220353911C>A , CM000664.1:g.220353911C>A	GRCh37
NC_000002.10:g.220062155C>A	NCBI36
NG_051022.1:g.59975C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8285C>A (SPEG) MANE Select	ENSP00000311684.7:p.Ser2762Tyr
ENST00000312358.11:c.8285C>A (SPEG)	ENSP00000311684.7:p.Ser2762Tyr
ENST00000485813.5:n.7528C>A (SPEG)
NM_005876.4:c.8285C>A (SPEG)	NP_005867.3:p.Ser2762Tyr
XM_005246237.2:c.8003C>A (SPEG)	XP_005246294.1:p.Ser2668Tyr
XM_005246239.2:c.5909C>A (SPEG)	XP_005246296.1:p.Ser1970Tyr
XM_005246240.2:c.5738C>A (SPEG)	XP_005246297.1:p.Ser1913Tyr
XM_005246241.1:c.5738C>A (SPEG)	XP_005246298.1:p.Ser1913Tyr
XM_005246242.3:c.5924C>A (SPEG)	XP_005246299.1:p.Ser1975Tyr
XM_006712189.2:c.7973C>A (SPEG)	XP_006712252.1:p.Ser2658Tyr
XM_006712193.2:c.5738C>A (SPEG)	XP_006712256.1:p.Ser1913Tyr
XM_011510479.1:c.8315C>A (SPEG)	XP_011508781.1:p.Ser2772Tyr
XM_011510480.1:c.8147C>A (SPEG)	XP_011508782.1:p.Ser2716Tyr
XM_011510481.1:c.8138C>A (SPEG)	XP_011508783.1:p.Ser2713Tyr
XM_011510482.1:c.8132C>A (SPEG)	XP_011508784.1:p.Ser2711Tyr
XM_011510483.1:c.8054C>A (SPEG)	XP_011508785.1:p.Ser2685Tyr
XM_011510484.1:c.7970C>A (SPEG)	XP_011508786.1:p.Ser2657Tyr
XR_923921.1:n.353-6780G>T (ASIC4-AS1)
XM_005246242.4:c.5924C>A (SPEG)	XP_005246299.1:p.Ser1975Tyr
XM_006712189.3:c.7973C>A (SPEG)	XP_006712252.1:p.Ser2658Tyr
XM_006712193.3:c.5738C>A (SPEG)	XP_006712256.1:p.Ser1913Tyr
XM_011510479.2:c.8315C>A (SPEG)	XP_011508781.1:p.Ser2772Tyr
XM_011510483.2:c.8033C>A (SPEG)	XP_011508785.2:p.Ser2678Tyr
XM_017003157.1:c.8033C>A (SPEG)	XP_016858646.1:p.Ser2678Tyr
XM_017003158.2:c.5738C>A (SPEG)	XP_016858647.1:p.Ser1913Tyr
XM_017003160.1:c.3293C>A (SPEG)	XP_016858649.1:p.Ser1098Tyr
XR_923921.2:n.392-6780G>T (ASIC4-AS1)
NM_005876.5:c.8285C>A (SPEG) MANE Select	NP_005867.3:p.Ser2762Tyr