Canonical Allele Identifier: CA710128877

Gene: SERPINA12

Linked Data

• dbSNP Id: rs1344918227
• MyVariant Identifiers: chr14:g.94960035A>G (hg19) ; chr14:g.94493698A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94493698A>G , CM000676.2:g.94493698A>G	GRCh38
NC_000014.8:g.94960035A>G , CM000676.1:g.94960035A>G	GRCh37
NC_000014.7:g.94029788A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677451.1:c.905+2675T>C MANE Select	ENSP00000503935.1:n.905+2675T>C
ENST00000341228.2:c.905+2675T>C	ENSP00000342109.2:n.905+2675T>C
ENST00000556881.5:c.905+2675T>C	ENSP00000451738.1:n.905+2675T>C
NM_001304461.1:c.905+2675T>C	NP_001291390.1:n.905+2675T>C
NM_173850.3:c.905+2675T>C	NP_776249.1:n.905+2675T>C
XM_011536451.1:c.905+2675T>C	XP_011534753.1:n.905+2675T>C
XM_011536452.1:c.905+2675T>C	XP_011534754.1:n.905+2675T>C
XM_011536453.1:c.905+2675T>C	XP_011534755.1:n.905+2675T>C
XM_011536454.1:c.905+2675T>C	XP_011534756.1:n.905+2675T>C
XM_011536455.1:c.905+2675T>C	XP_011534757.1:n.905+2675T>C
XM_011536451.3:c.905+2675T>C	XP_011534753.1:n.905+2675T>C
XM_011536452.3:c.905+2675T>C	XP_011534754.1:n.905+2675T>C
XM_011536453.2:c.905+2675T>C	XP_011534755.1:n.905+2675T>C
XM_011536454.3:c.905+2675T>C	XP_011534756.1:n.905+2675T>C
XM_017020989.2:c.905+2675T>C	XP_016876478.1:n.905+2675T>C
XM_017020990.1:c.905+2675T>C	XP_016876479.1:n.905+2675T>C
NM_001304461.2:c.905+2675T>C	NP_001291390.1:n.905+2675T>C
NM_173850.4:c.905+2675T>C	NP_776249.1:n.905+2675T>C
NM_001382267.1:c.905+2675T>C MANE Select	NP_001369196.1:n.905+2675T>C