Canonical Allele Identifier: CA5158332
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 531619
dbSNP Id: rs200546215

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.100252315A>G , CM000671.2:g.100252315A>G GRCh38
NC_000009.11:g.103014597A>G , CM000671.1:g.103014597A>G GRCh37
NC_000009.10:g.102054418A>G NCBI36
NG_008316.1:g.158087A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262457.7:c.1111A>G MANE Select ENSP00000262457.2:p.Ser371Gly
ENST00000262456.6:c.1111A>G ENSP00000262456.2:p.Ser371Gly
ENST00000262457.6:c.1111A>G ENSP00000262457.2:p.Ser371Gly
NM_014425.3:c.1111A>G NP_055240.2:p.Ser371Gly
NM_183245.2:c.1111A>G NP_899068.1:p.Ser371Gly
NR_051962.1:n.1420A>G
XM_005251923.3:c.1111A>G XP_005251980.1:p.Ser371Gly
XM_005251924.3:c.823A>G XP_005251981.1:p.Ser275Gly
XM_011518531.1:c.1111A>G XP_011516833.1:p.Ser371Gly
XM_011518532.1:c.1111A>G XP_011516834.1:p.Ser371Gly
XM_011518533.1:c.1111A>G XP_011516835.1:p.Ser371Gly
XM_011518534.1:c.823A>G XP_011516836.1:p.Ser275Gly
XM_011518535.1:c.823A>G XP_011516837.1:p.Ser275Gly
XM_011518536.1:c.823A>G XP_011516838.1:p.Ser275Gly
XM_011518537.1:c.823A>G XP_011516839.1:p.Ser275Gly
XM_011518538.1:c.823A>G XP_011516840.1:p.Ser275Gly
XM_011518539.1:c.790A>G XP_011516841.1:p.Ser264Gly
XM_011518540.1:c.790A>G XP_011516842.1:p.Ser264Gly
XM_011518541.1:c.790A>G XP_011516843.1:p.Ser264Gly
XM_011518542.1:c.823A>G XP_011516844.1:p.Ser275Gly
XM_011518543.1:c.133A>G XP_011516845.1:p.Ser45Gly
XM_011518544.1:c.133A>G XP_011516846.1:p.Ser45Gly
XR_242585.1:n.1367A>G
XR_242586.1:n.1367A>G
XR_428522.1:n.1367A>G
NM_001318381.1:c.823A>G NP_001305310.1:p.Ser275Gly
NM_001318382.1:c.133A>G NP_001305311.1:p.Ser45Gly
NM_014425.4:c.1111A>G NP_055240.2:p.Ser371Gly
NR_134606.1:n.1367A>G
NM_014425.5:c.1111A>G MANE Select NP_055240.2:p.Ser371Gly
NM_001318381.2:c.823A>G NP_001305310.1:p.Ser275Gly
NM_001318382.2:c.133A>G NP_001305311.1:p.Ser45Gly
NR_134606.2:n.1309A>G