Canonical Allele Identifier: CA710133606

Gene: SERPINA3

Linked Data

• dbSNP Id: rs1307004255
• gnomAD v3: 14-94619585-T-C
• gnomAD v4: 14-94619585-T-C
• MyVariant Identifiers: chr14:g.95085922T>C (hg19) ; chr14:g.94619585T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94619585T>C , CM000676.2:g.94619585T>C	GRCh38
NC_000014.8:g.95085922T>C , CM000676.1:g.95085922T>C	GRCh37
NC_000014.7:g.94155675T>C	NCBI36
NG_012879.1:g.12209T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393078.5:c.917+117T>C MANE Select	ENSP00000376793.3:n.917+117T>C
ENST00000393078.4:c.917+117T>C	ENSP00000376793.3:n.917+117T>C
ENST00000393080.8:c.917+117T>C	ENSP00000376795.4:n.917+117T>C
ENST00000467132.5:c.917+117T>C	ENSP00000450540.1:n.917+117T>C
ENST00000482740.2:c.263+117T>C	ENSP00000451119.1:n.263+117T>C
ENST00000553947.1:c.1880+117T>C
ENST00000556388.1:n.58-2756T>C
ENST00000556968.2:c.644-2756T>C	ENSP00000452476.1:n.644-2756T>C
ENST00000621603.1:c.253T>C
NM_001085.4:c.917+117T>C	NP_001076.2:n.917+117T>C
NM_001085.5:c.917+117T>C MANE Select	NP_001076.2:n.917+117T>C
NM_001384672.1:c.917+117T>C	NP_001371601.1:n.917+117T>C
NM_001384673.1:c.917+117T>C	NP_001371602.1:n.917+117T>C
NM_001384674.1:c.917+117T>C	NP_001371603.1:n.917+117T>C