Canonical Allele Identifier: CA10646638

Gene: SERPINA1

Linked Data

• ClinVar Variation Id: 315034
• ClinVar RCV Id: RCV000597167 ; RCV000383822
• dbSNP Id: rs11558258
• gnomAD v2: 14-94854902-A-G
• gnomAD v3: 14-94388565-A-G
• gnomAD v4: 14-94388565-A-G
• MyVariant Identifiers: chr14:g.94854902A>G (hg19) ; chr14:g.94388565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94388565A>G , CM000676.2:g.94388565A>G	GRCh38
NC_000014.8:g.94854902A>G , CM000676.1:g.94854902A>G	GRCh37
NC_000014.7:g.93924655A>G	NCBI36
NG_008290.1:g.7128T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393087.9:c.-10T>C MANE Select	ENSP00000376802.4:n.-10T>C
ENST00000636712.1:c.-10T>C	ENSP00000490054.1:n.-10T>C
ENST00000355814.8:c.-5+1855T>C	ENSP00000348068.4:n.-5+1855T>C
ENST00000393087.8:c.-10T>C	ENSP00000376802.4:n.-10T>C
ENST00000393088.8:c.-10T>C	ENSP00000376803.4:n.-10T>C
ENST00000402629.1:c.-10T>C	ENSP00000386094.1:n.-10T>C
ENST00000404814.8:c.-10T>C	ENSP00000385960.4:n.-10T>C
ENST00000437397.5:c.-10T>C	ENSP00000408474.1:n.-10T>C
ENST00000440909.5:c.-5+1892T>C	ENSP00000390299.1:n.-5+1892T>C
ENST00000448921.5:c.-10T>C	ENSP00000416066.1:n.-10T>C
ENST00000449399.7:c.-10T>C	ENSP00000416354.3:n.-10T>C
ENST00000553327.5:c.-10T>C	ENSP00000452480.1:n.-10T>C
ENST00000554720.1:c.-29T>C	ENSP00000450561.1:n.-29T>C
ENST00000555289.5:n.488T>C
ENST00000556091.1:c.-148T>C	ENSP00000452169.1:n.-148T>C
ENST00000556955.5:c.-5+1855T>C	ENSP00000451098.1:n.-5+1855T>C
ENST00000557118.5:c.-10T>C	ENSP00000451826.1:n.-10T>C
ENST00000557492.5:c.-10T>C	ENSP00000452452.1:n.-10T>C
NM_000295.4:c.-10T>C	NP_000286.3:n.-10T>C
NM_001002235.2:c.-5+1892T>C	NP_001002235.1:n.-5+1892T>C
NM_001002236.2:c.-10T>C	NP_001002236.1:n.-10T>C
NM_001127700.1:c.-5+1855T>C	NP_001121172.1:n.-5+1855T>C
NM_001127701.1:c.-10T>C	NP_001121173.1:n.-10T>C
NM_001127702.1:c.-10T>C	NP_001121174.1:n.-10T>C
NM_001127703.1:c.-10T>C	NP_001121175.1:n.-10T>C
NM_001127704.1:c.-10T>C	NP_001121176.1:n.-10T>C
NM_001127705.1:c.-10T>C	NP_001121177.1:n.-10T>C
NM_001127706.1:c.-10T>C	NP_001121178.1:n.-10T>C
NM_001127707.1:c.-10T>C	NP_001121179.1:n.-10T>C
XM_017021370.1:c.-148T>C	XP_016876859.1:n.-148T>C
NM_000295.5:c.-10T>C MANE Select	NP_000286.3:n.-10T>C
NM_001002235.3:c.-5+1892T>C	NP_001002235.1:n.-5+1892T>C
NM_001002236.3:c.-10T>C	NP_001002236.1:n.-10T>C
NM_001127700.2:c.-5+1855T>C	NP_001121172.1:n.-5+1855T>C
NM_001127701.2:c.-10T>C	NP_001121173.1:n.-10T>C
NM_001127702.2:c.-10T>C	NP_001121174.1:n.-10T>C
NM_001127703.2:c.-10T>C	NP_001121175.1:n.-10T>C
NM_001127704.2:c.-10T>C	NP_001121176.1:n.-10T>C
NM_001127705.2:c.-10T>C	NP_001121177.1:n.-10T>C
NM_001127706.2:c.-10T>C	NP_001121178.1:n.-10T>C
NM_001127707.2:c.-10T>C	NP_001121179.1:n.-10T>C