Canonical Allele Identifier: CA615829855

Gene: SERPINA1

Linked Data

• dbSNP Id: rs1474075943
• gnomAD v2: 14-94845016-T-TGCCCCAG
• gnomAD v3: 14-94378679-T-TGCCCCAG
• gnomAD v4: 14-94378679-T-TGCCCCAG
• MyVariant Identifiers: chr14:g.94845016_94845017insGCCCCAG (hg19) ; chr14:g.94378679_94378680insGCCCCAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94378679_94378680insGCCCCAG , CM000676.2:g.94378679_94378680insGCCCCAG	GRCh38
NC_000014.8:g.94845016_94845017insGCCCCAG , CM000676.1:g.94845016_94845017insGCCCCAG	GRCh37
NC_000014.7:g.93914769_93914770insGCCCCAG	NCBI36
NG_008290.1:g.17013_17014insCTGGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393087.9:c.1066-40_1066-39insCTGGGGC MANE Select	ENSP00000376802.4:n.1066-40_1066-39insCTGGGGC
ENST00000636712.1:c.1066-40_1066-39insCTGGGGC	ENSP00000490054.1:n.1066-40_1066-39insCTGGGGC
ENST00000355814.8:c.1066-40_1066-39insCTGGGGC	ENSP00000348068.4:n.1066-40_1066-39insCTGGGGC
ENST00000393087.8:c.1066-40_1066-39insCTGGGGC	ENSP00000376802.4:n.1066-40_1066-39insCTGGGGC
ENST00000393088.8:c.1066-40_1066-39insCTGGGGC	ENSP00000376803.4:n.1066-40_1066-39insCTGGGGC
ENST00000404814.8:c.1066-40_1066-39insCTGGGGC	ENSP00000385960.4:n.1066-40_1066-39insCTGGGGC
ENST00000437397.5:c.1066-40_1066-39insCTGGGGC	ENSP00000408474.1:n.1066-40_1066-39insCTGGGGC
ENST00000440909.5:c.1066-40_1066-39insCTGGGGC	ENSP00000390299.1:n.1066-40_1066-39insCTGGGGC
ENST00000448921.5:c.1066-40_1066-39insCTGGGGC	ENSP00000416066.1:n.1066-40_1066-39insCTGGGGC
ENST00000449399.7:c.1066-40_1066-39insCTGGGGC	ENSP00000416354.3:n.1066-40_1066-39insCTGGGGC
ENST00000489769.1:c.*365-40_*365-39insCTGGGGC	ENSP00000451525.1:n.*365-40_*365-39insCTGGGGC
NM_000295.4:c.1066-40_1066-39insCTGGGGC	NP_000286.3:n.1066-40_1066-39insCTGGGGC
NM_001002235.2:c.1066-40_1066-39insCTGGGGC	NP_001002235.1:n.1066-40_1066-39insCTGGGGC
NM_001002236.2:c.1066-40_1066-39insCTGGGGC	NP_001002236.1:n.1066-40_1066-39insCTGGGGC
NM_001127700.1:c.1066-40_1066-39insCTGGGGC	NP_001121172.1:n.1066-40_1066-39insCTGGGGC
NM_001127701.1:c.1066-40_1066-39insCTGGGGC	NP_001121173.1:n.1066-40_1066-39insCTGGGGC
NM_001127702.1:c.1066-40_1066-39insCTGGGGC	NP_001121174.1:n.1066-40_1066-39insCTGGGGC
NM_001127703.1:c.1066-40_1066-39insCTGGGGC	NP_001121175.1:n.1066-40_1066-39insCTGGGGC
NM_001127704.1:c.1066-40_1066-39insCTGGGGC	NP_001121176.1:n.1066-40_1066-39insCTGGGGC
NM_001127705.1:c.1066-40_1066-39insCTGGGGC	NP_001121177.1:n.1066-40_1066-39insCTGGGGC
NM_001127706.1:c.1066-40_1066-39insCTGGGGC	NP_001121178.1:n.1066-40_1066-39insCTGGGGC
NM_001127707.1:c.1066-40_1066-39insCTGGGGC	NP_001121179.1:n.1066-40_1066-39insCTGGGGC
XM_017021370.1:c.1066-40_1066-39insCTGGGGC	XP_016876859.1:n.1066-40_1066-39insCTGGGGC
NM_000295.5:c.1066-40_1066-39insCTGGGGC MANE Select	NP_000286.3:n.1066-40_1066-39insCTGGGGC
NM_001002235.3:c.1066-40_1066-39insCTGGGGC	NP_001002235.1:n.1066-40_1066-39insCTGGGGC
NM_001002236.3:c.1066-40_1066-39insCTGGGGC	NP_001002236.1:n.1066-40_1066-39insCTGGGGC
NM_001127700.2:c.1066-40_1066-39insCTGGGGC	NP_001121172.1:n.1066-40_1066-39insCTGGGGC
NM_001127701.2:c.1066-40_1066-39insCTGGGGC	NP_001121173.1:n.1066-40_1066-39insCTGGGGC
NM_001127702.2:c.1066-40_1066-39insCTGGGGC	NP_001121174.1:n.1066-40_1066-39insCTGGGGC
NM_001127703.2:c.1066-40_1066-39insCTGGGGC	NP_001121175.1:n.1066-40_1066-39insCTGGGGC
NM_001127704.2:c.1066-40_1066-39insCTGGGGC	NP_001121176.1:n.1066-40_1066-39insCTGGGGC
NM_001127705.2:c.1066-40_1066-39insCTGGGGC	NP_001121177.1:n.1066-40_1066-39insCTGGGGC
NM_001127706.2:c.1066-40_1066-39insCTGGGGC	NP_001121178.1:n.1066-40_1066-39insCTGGGGC
NM_001127707.2:c.1066-40_1066-39insCTGGGGC	NP_001121179.1:n.1066-40_1066-39insCTGGGGC