Canonical Allele Identifier: CA2156010736
Gene: SERPINA12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94493723A= , CM000676.2:g.94493723A= GRCh38
NC_000014.8:g.94960060A= , CM000676.1:g.94960060A= GRCh37
NC_000014.7:g.94029813A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000677451.1:c.905+2650T= MANE Select ENSP00000503935.1:n.905+2650T=
ENST00000341228.2:c.905+2650T= ENSP00000342109.2:n.905+2650T=
ENST00000556881.5:c.905+2650T= ENSP00000451738.1:n.905+2650T=
NM_001304461.1:c.905+2650T= NP_001291390.1:n.905+2650T=
NM_173850.3:c.905+2650T= NP_776249.1:n.905+2650T=
XM_011536451.1:c.905+2650T= XP_011534753.1:n.905+2650T=
XM_011536452.1:c.905+2650T= XP_011534754.1:n.905+2650T=
XM_011536453.1:c.905+2650T= XP_011534755.1:n.905+2650T=
XM_011536454.1:c.905+2650T= XP_011534756.1:n.905+2650T=
XM_011536455.1:c.905+2650T= XP_011534757.1:n.905+2650T=
XM_011536451.3:c.905+2650T= XP_011534753.1:n.905+2650T=
XM_011536452.3:c.905+2650T= XP_011534754.1:n.905+2650T=
XM_011536453.2:c.905+2650T= XP_011534755.1:n.905+2650T=
XM_011536454.3:c.905+2650T= XP_011534756.1:n.905+2650T=
XM_017020989.2:c.905+2650T= XP_016876478.1:n.905+2650T=
XM_017020990.1:c.905+2650T= XP_016876479.1:n.905+2650T=
NM_001304461.2:c.905+2650T= NP_001291390.1:n.905+2650T=
NM_173850.4:c.905+2650T= NP_776249.1:n.905+2650T=
NM_001382267.1:c.905+2650T= MANE Select NP_001369196.1:n.905+2650T=