Canonical Allele Identifier: CA2156010662

Gene: SERPINA12

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94493619_94493663delinsACCACTGAGAGCAGCCTACACTCTACACTTGGACTTCACGAGACG , CM000676.2:g.94493619_94493663delinsACCACTGAGAGCAGCCTACACTCTACACTTGGACTTCACGAGACG	GRCh38
NC_000014.8:g.94959956_94960000delinsACCACTGAGAGCAGCCTACACTCTACACTTGGACTTCACGAGACG , CM000676.1:g.94959956_94960000delinsACCACTGAGAGCAGCCTACACTCTACACTTGGACTTCACGAGACG	GRCh37
NC_000014.7:g.94029709_94029753delinsACCACTGAGAGCAGCCTACACTCTACACTTGGACTTCACGAGACG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677451.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT MANE Select	ENSP00000503935.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAG...
ENST00000341228.2:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	ENSP00000342109.2:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAG...
ENST00000556881.5:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	ENSP00000451738.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAG...
NM_001304461.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	NP_001291390.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
NM_173850.3:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	NP_776249.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGA...
XM_011536451.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534753.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_011536452.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534754.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_011536453.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534755.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_011536454.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534756.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_011536455.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534757.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_011536451.3:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534753.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_011536452.3:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534754.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_011536453.2:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534755.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_011536454.3:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_011534756.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_017020989.2:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_016876478.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
XM_017020990.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	XP_016876479.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
NM_001304461.2:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	NP_001291390.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...
NM_173850.4:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT	NP_776249.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGA...
NM_001382267.1:c.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGTAGAGTGTAGGCTGCTCTCAGTGGT MANE Select	NP_001369196.1:n.905+2710_905+2754delinsCGTCTCGTGAAGTCCAAGTGT...