Canonical Allele Identifier: CA350708875

Gene: SPEG ASIC4-AS1

Linked Data

• MyVariant Identifiers: chr2:g.220353945T>C (hg19) ; chr2:g.219489223T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489223T>C , CM000664.2:g.219489223T>C	GRCh38
NC_000002.11:g.220353945T>C , CM000664.1:g.220353945T>C	GRCh37
NC_000002.10:g.220062189T>C	NCBI36
NG_051022.1:g.60009T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8317+2T>C (SPEG) MANE Select	ENSP00000311684.7:n.8317+2T>C
ENST00000312358.11:c.8317+2T>C (SPEG)	ENSP00000311684.7:n.8317+2T>C
ENST00000485813.5:n.7560+2T>C (SPEG)
NM_005876.4:c.8317+2T>C (SPEG)	NP_005867.3:n.8317+2T>C
XM_005246237.2:c.8035+2T>C (SPEG)	XP_005246294.1:n.8035+2T>C
XM_005246239.2:c.5941+2T>C (SPEG)	XP_005246296.1:n.5941+2T>C
XM_005246240.2:c.5770+2T>C (SPEG)	XP_005246297.1:n.5770+2T>C
XM_005246241.1:c.5770+2T>C (SPEG)	XP_005246298.1:n.5770+2T>C
XM_005246242.3:c.5956+2T>C (SPEG)	XP_005246299.1:n.5956+2T>C
XM_006712189.2:c.8005+2T>C (SPEG)	XP_006712252.1:n.8005+2T>C
XM_006712193.2:c.5770+2T>C (SPEG)	XP_006712256.1:n.5770+2T>C
XM_011510479.1:c.8347+2T>C (SPEG)	XP_011508781.1:n.8347+2T>C
XM_011510480.1:c.8179+2T>C (SPEG)	XP_011508782.1:n.8179+2T>C
XM_011510481.1:c.8170+2T>C (SPEG)	XP_011508783.1:n.8170+2T>C
XM_011510482.1:c.8164+2T>C (SPEG)	XP_011508784.1:n.8164+2T>C
XM_011510483.1:c.8086+2T>C (SPEG)	XP_011508785.1:n.8086+2T>C
XM_011510484.1:c.8002+2T>C (SPEG)	XP_011508786.1:n.8002+2T>C
XR_923921.1:n.353-6814A>G (ASIC4-AS1)
XM_005246242.4:c.5956+2T>C (SPEG)	XP_005246299.1:n.5956+2T>C
XM_006712189.3:c.8005+2T>C (SPEG)	XP_006712252.1:n.8005+2T>C
XM_006712193.3:c.5770+2T>C (SPEG)	XP_006712256.1:n.5770+2T>C
XM_011510479.2:c.8347+2T>C (SPEG)	XP_011508781.1:n.8347+2T>C
XM_011510483.2:c.8065+2T>C (SPEG)	XP_011508785.2:n.8065+2T>C
XM_017003157.1:c.8065+2T>C (SPEG)	XP_016858646.1:n.8065+2T>C
XM_017003158.2:c.5770+2T>C (SPEG)	XP_016858647.1:n.5770+2T>C
XM_017003160.1:c.3325+2T>C (SPEG)	XP_016858649.1:n.3325+2T>C
XR_923921.2:n.392-6814A>G (ASIC4-AS1)
NM_005876.5:c.8317+2T>C (SPEG) MANE Select	NP_005867.3:n.8317+2T>C