Canonical Allele Identifier: CA324628446

Gene: SHISA8

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41909874C>G , CM000684.2:g.41909874C>G	GRCh38
NC_000022.10:g.42305878C>G , CM000684.1:g.42305878C>G	GRCh37
NC_000022.9:g.40635824C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001207020.3:c.1085G>C MANE Select	NP_001193949.1:p.Ser362Thr
ENST00000621082.2:c.1085G>C MANE Select	ENSP00000481203.1:p.Ser362Thr
NM_001207020.1:c.1085G>C	NP_001193949.1:p.Ser362Thr
NM_001207020.2:c.1085G>C	NP_001193949.1:p.Ser362Thr
NM_001353438.1:c.1370G>C	NP_001340367.1:p.Ser457Thr
NM_001353438.2:c.1370G>C	NP_001340367.1:p.Ser457Thr
NM_001353439.1:c.1262G>C	NP_001340368.1:p.Ser421Thr
NM_001353439.2:c.1262G>C	NP_001340368.1:p.Ser421Thr
ENST00000621082.1:c.1085G>C	ENSP00000481203.1:p.Ser362Thr
XM_006724254.2:c.1370G>C	XP_006724317.1:p.Ser457Thr
XM_006724255.2:c.1262G>C	XP_006724318.1:p.Ser421Thr
XM_006724256.2:c.1250G>C	XP_006724319.1:p.Ser417Thr
XM_006724256.4:c.1250G>C	XP_006724319.1:p.Ser417Thr
XR_002958691.1:n.1796G>C