Canonical Allele Identifier: CA2156010698
Gene: SERPINA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94493658_94493695delinsGAGACGCCACTGAGAGCAGCTTACACTTGGACTTCACA , CM000676.2:g.94493658_94493695delinsGAGACGCCACTGAGAGCAGCTTACACTTGGACTTCACA GRCh38
NC_000014.8:g.94959995_94960032delinsGAGACGCCACTGAGAGCAGCTTACACTTGGACTTCACA , CM000676.1:g.94959995_94960032delinsGAGACGCCACTGAGAGCAGCTTACACTTGGACTTCACA GRCh37
NC_000014.7:g.94029748_94029785delinsGAGACGCCACTGAGAGCAGCTTACACTTGGACTTCACA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000677451.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC MANE Select ENSP00000503935.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAA...
ENST00000341228.2:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC ENSP00000342109.2:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAA...
ENST00000556881.5:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC ENSP00000451738.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAA...
NM_001304461.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC NP_001291390.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
NM_173850.3:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC NP_776249.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCT...
XM_011536451.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534753.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_011536452.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534754.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_011536453.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534755.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_011536454.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534756.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_011536455.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534757.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_011536451.3:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534753.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_011536452.3:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534754.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_011536453.2:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534755.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_011536454.3:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_011534756.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_017020989.2:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_016876478.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
XM_017020990.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC XP_016876479.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
NM_001304461.2:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC NP_001291390.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...
NM_173850.4:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC NP_776249.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCT...
NM_001382267.1:c.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCTGCTCTCAGTGGCGTCTC MANE Select NP_001369196.1:n.905+2678_905+2715delinsTGTGAAGTCCAAGTGTAAGCT...