Canonical Allele Identifier: CA2156010687
Gene: SERPINA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94493641_94493678delinsCTACACTTGGACTTCACGAGACGCCACTGAGAGCAGCT , CM000676.2:g.94493641_94493678delinsCTACACTTGGACTTCACGAGACGCCACTGAGAGCAGCT GRCh38
NC_000014.8:g.94959978_94960015delinsCTACACTTGGACTTCACGAGACGCCACTGAGAGCAGCT , CM000676.1:g.94959978_94960015delinsCTACACTTGGACTTCACGAGACGCCACTGAGAGCAGCT GRCh37
NC_000014.7:g.94029731_94029768delinsCTACACTTGGACTTCACGAGACGCCACTGAGAGCAGCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000677451.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG MANE Select ENSP00000503935.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGT...
ENST00000341228.2:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG ENSP00000342109.2:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGT...
ENST00000556881.5:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG ENSP00000451738.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGT...
NM_001304461.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG NP_001291390.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
NM_173850.3:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG NP_776249.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTG...
XM_011536451.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534753.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_011536452.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534754.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_011536453.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534755.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_011536454.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534756.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_011536455.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534757.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_011536451.3:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534753.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_011536452.3:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534754.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_011536453.2:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534755.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_011536454.3:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_011534756.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_017020989.2:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_016876478.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
XM_017020990.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG XP_016876479.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
NM_001304461.2:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG NP_001291390.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...
NM_173850.4:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG NP_776249.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTG...
NM_001382267.1:c.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTCGTGAAGTCCAAGTGTAG MANE Select NP_001369196.1:n.905+2695_905+2732delinsAGCTGCTCTCAGTGGCGTCTC...