Canonical Allele Identifier: CA397590202
Community Standard Title: NM_002615.7(SERPINF1):c.998-2A>G
Gene: SERPINF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1777185A>G , CM000679.2:g.1777185A>G GRCh38
NC_000017.10:g.1680479A>G , CM000679.1:g.1680479A>G GRCh37
NC_000017.9:g.1627229A>G NCBI36
NG_028180.1:g.20221A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002615.7:c.998-2A>G MANE Select NP_002606.3:n.998-2A>G
ENST00000254722.9:c.998-2A>G MANE Select ENSP00000254722.4:n.998-2A>G
NM_001329903.1:c.998-2A>G NP_001316832.1:n.998-2A>G
NM_001329903.2:c.998-2A>G NP_001316832.1:n.998-2A>G
NM_001329904.1:c.437-2A>G NP_001316833.1:n.437-2A>G
NM_001329904.2:c.437-2A>G NP_001316833.1:n.437-2A>G
NM_001329905.1:c.437-2A>G NP_001316834.1:n.437-2A>G
NM_001329905.2:c.437-2A>G NP_001316834.1:n.437-2A>G
NM_002615.5:c.998-2A>G NP_002606.3:n.998-2A>G
NM_002615.6:c.998-2A>G NP_002606.3:n.998-2A>G
ENST00000254722.8:c.998-2A>G ENSP00000254722.4:n.998-2A>G
ENST00000572517.1:n.294-2A>G
ENST00000573763.1:c.392-2A>G ENSP00000461405.1:n.392-2A>G