Canonical Allele Identifier: CA196896138
Community Standard Title: NM_014425.5(INVS):c.2719C>G (p.Arg907Gly)
Gene: INVS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.100292976C>G , CM000671.2:g.100292976C>G GRCh38
NC_000009.11:g.103055258C>G , CM000671.1:g.103055258C>G GRCh37
NC_000009.10:g.102095079C>G NCBI36
NG_008316.1:g.198748C>G

Transcript Alleles

HGVS Amino-acid Change
NM_014425.5:c.2719C>G MANE Select NP_055240.2:p.Arg907Gly
ENST00000262457.7:c.2719C>G MANE Select ENSP00000262457.2:p.Arg907Gly
NM_001318381.1:c.2431C>G NP_001305310.1:p.Arg811Gly
NM_001318381.2:c.2431C>G NP_001305310.1:p.Arg811Gly
NM_001318382.1:c.1741C>G NP_001305311.1:p.Arg581Gly
NM_001318382.2:c.1741C>G NP_001305311.1:p.Arg581Gly
NM_014425.3:c.2719C>G NP_055240.2:p.Arg907Gly
NM_014425.4:c.2719C>G NP_055240.2:p.Arg907Gly
NM_183245.2:c.2209C>G NP_899068.1:p.Arg737Gly
NR_051962.1:n.3028C>G
NR_134606.1:n.2926C>G
NR_134606.2:n.2868C>G
ENST00000262456.6:c.2209C>G ENSP00000262456.2:p.Arg737Gly
ENST00000262457.6:c.2719C>G ENSP00000262457.2:p.Arg907Gly
XM_005251923.3:c.2719C>G XP_005251980.1:p.Arg907Gly
XM_005251924.3:c.2431C>G XP_005251981.1:p.Arg811Gly
XM_011518531.1:c.2719C>G XP_011516833.1:p.Arg907Gly
XM_011518532.1:c.2719C>G XP_011516834.1:p.Arg907Gly
XM_011518533.1:c.2719C>G XP_011516835.1:p.Arg907Gly
XM_011518534.1:c.2431C>G XP_011516836.1:p.Arg811Gly
XM_011518535.1:c.2431C>G XP_011516837.1:p.Arg811Gly
XM_011518536.1:c.2431C>G XP_011516838.1:p.Arg811Gly
XM_011518537.1:c.2431C>G XP_011516839.1:p.Arg811Gly
XM_011518538.1:c.2431C>G XP_011516840.1:p.Arg811Gly
XM_011518539.1:c.2398C>G XP_011516841.1:p.Arg800Gly
XM_011518540.1:c.2398C>G XP_011516842.1:p.Arg800Gly
XM_011518541.1:c.2398C>G XP_011516843.1:p.Arg800Gly
XM_011518542.1:c.1921C>G XP_011516844.1:p.Arg641Gly
XM_011518543.1:c.1741C>G XP_011516845.1:p.Arg581Gly
XM_011518544.1:c.1741C>G XP_011516846.1:p.Arg581Gly
XR_242585.1:n.2902C>G
XR_242586.1:n.2926C>G
XR_428522.1:n.2416C>G