Canonical Allele Identifier: CA2635276381

Gene: SERPINF1

Linked Data

• gnomAD v4: 17-1772096-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772096T>C , CM000679.2:g.1772096T>C	GRCh38
NC_000017.10:g.1675390T>C , CM000679.1:g.1675390T>C	GRCh37
NC_000017.9:g.1622140T>C	NCBI36
NG_028180.1:g.15132T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.643+21T>C MANE Select	ENSP00000254722.4:n.643+21T>C
ENST00000254722.8:c.643+21T>C	ENSP00000254722.4:n.643+21T>C
ENST00000572048.1:c.82+21T>C	ENSP00000458484.1:n.82+21T>C
ENST00000573763.1:c.42+21T>C	ENSP00000461405.1:n.42+21T>C
ENST00000576406.5:c.82+21T>C	ENSP00000461214.1:n.82+21T>C
NM_002615.5:c.643+21T>C	NP_002606.3:n.643+21T>C
NM_001329903.1:c.643+21T>C	NP_001316832.1:n.643+21T>C
NM_001329904.1:c.82+21T>C	NP_001316833.1:n.82+21T>C
NM_001329905.1:c.82+21T>C	NP_001316834.1:n.82+21T>C
NM_002615.6:c.643+21T>C	NP_002606.3:n.643+21T>C
NM_002615.7:c.643+21T>C MANE Select	NP_002606.3:n.643+21T>C
NM_001329903.2:c.643+21T>C	NP_001316832.1:n.643+21T>C
NM_001329904.2:c.82+21T>C	NP_001316833.1:n.82+21T>C
NM_001329905.2:c.82+21T>C	NP_001316834.1:n.82+21T>C