Canonical Allele Identifier: CA350708778

Gene: SPEG ASIC4-AS1

Linked Data

• MyVariant Identifiers: chr2:g.220353902T>C (hg19) ; chr2:g.219489180T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489180T>C , CM000664.2:g.219489180T>C	GRCh38
NC_000002.11:g.220353902T>C , CM000664.1:g.220353902T>C	GRCh37
NC_000002.10:g.220062146T>C	NCBI36
NG_051022.1:g.59966T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8276T>C (SPEG) MANE Select	ENSP00000311684.7:p.Phe2759Ser
ENST00000312358.11:c.8276T>C (SPEG)	ENSP00000311684.7:p.Phe2759Ser
ENST00000485813.5:n.7519T>C (SPEG)
NM_005876.4:c.8276T>C (SPEG)	NP_005867.3:p.Phe2759Ser
XM_005246237.2:c.7994T>C (SPEG)	XP_005246294.1:p.Phe2665Ser
XM_005246239.2:c.5900T>C (SPEG)	XP_005246296.1:p.Phe1967Ser
XM_005246240.2:c.5729T>C (SPEG)	XP_005246297.1:p.Phe1910Ser
XM_005246241.1:c.5729T>C (SPEG)	XP_005246298.1:p.Phe1910Ser
XM_005246242.3:c.5915T>C (SPEG)	XP_005246299.1:p.Phe1972Ser
XM_006712189.2:c.7964T>C (SPEG)	XP_006712252.1:p.Phe2655Ser
XM_006712193.2:c.5729T>C (SPEG)	XP_006712256.1:p.Phe1910Ser
XM_011510479.1:c.8306T>C (SPEG)	XP_011508781.1:p.Phe2769Ser
XM_011510480.1:c.8138T>C (SPEG)	XP_011508782.1:p.Phe2713Ser
XM_011510481.1:c.8129T>C (SPEG)	XP_011508783.1:p.Phe2710Ser
XM_011510482.1:c.8123T>C (SPEG)	XP_011508784.1:p.Phe2708Ser
XM_011510483.1:c.8045T>C (SPEG)	XP_011508785.1:p.Phe2682Ser
XM_011510484.1:c.7961T>C (SPEG)	XP_011508786.1:p.Phe2654Ser
XR_923921.1:n.353-6771A>G (ASIC4-AS1)
XM_005246242.4:c.5915T>C (SPEG)	XP_005246299.1:p.Phe1972Ser
XM_006712189.3:c.7964T>C (SPEG)	XP_006712252.1:p.Phe2655Ser
XM_006712193.3:c.5729T>C (SPEG)	XP_006712256.1:p.Phe1910Ser
XM_011510479.2:c.8306T>C (SPEG)	XP_011508781.1:p.Phe2769Ser
XM_011510483.2:c.8024T>C (SPEG)	XP_011508785.2:p.Phe2675Ser
XM_017003157.1:c.8024T>C (SPEG)	XP_016858646.1:p.Phe2675Ser
XM_017003158.2:c.5729T>C (SPEG)	XP_016858647.1:p.Phe1910Ser
XM_017003160.1:c.3284T>C (SPEG)	XP_016858649.1:p.Phe1095Ser
XR_923921.2:n.392-6771A>G (ASIC4-AS1)
NM_005876.5:c.8276T>C (SPEG) MANE Select	NP_005867.3:p.Phe2759Ser