Canonical Allele Identifier: CA2635276576
Gene: SERPINF1 HGNC NCBI

Linked Data

gnomAD v4: 17-1772173-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1772173G>T , CM000679.2:g.1772173G>T GRCh38
NC_000017.10:g.1675467G>T , CM000679.1:g.1675467G>T GRCh37
NC_000017.9:g.1622217G>T NCBI36
NG_028180.1:g.15209G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254722.9:c.643+98G>T MANE Select ENSP00000254722.4:n.643+98G>T
ENST00000254722.8:c.643+98G>T ENSP00000254722.4:n.643+98G>T
ENST00000572048.1:c.82+98G>T ENSP00000458484.1:n.82+98G>T
ENST00000573763.1:c.42+98G>T ENSP00000461405.1:n.42+98G>T
ENST00000576406.5:c.82+98G>T ENSP00000461214.1:n.82+98G>T
NM_002615.5:c.643+98G>T NP_002606.3:n.643+98G>T
NM_001329903.1:c.643+98G>T NP_001316832.1:n.643+98G>T
NM_001329904.1:c.82+98G>T NP_001316833.1:n.82+98G>T
NM_001329905.1:c.82+98G>T NP_001316834.1:n.82+98G>T
NM_002615.6:c.643+98G>T NP_002606.3:n.643+98G>T
NM_002615.7:c.643+98G>T MANE Select NP_002606.3:n.643+98G>T
NM_001329903.2:c.643+98G>T NP_001316832.1:n.643+98G>T
NM_001329904.2:c.82+98G>T NP_001316833.1:n.82+98G>T
NM_001329905.2:c.82+98G>T NP_001316834.1:n.82+98G>T