Canonical Allele Identifier: CA2580092453
Community Standard Title: NM_002615.7(SERPINF1):c.787-10C>G
Gene: SERPINF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1776522C>G , CM000679.2:g.1776522C>G GRCh38
NC_000017.10:g.1679816C>G , CM000679.1:g.1679816C>G GRCh37
NC_000017.9:g.1626566C>G NCBI36
NG_028180.1:g.19558C>G

Transcript Alleles

HGVS Amino-acid Change
NM_002615.7:c.787-10C>G MANE Select NP_002606.3:n.787-10C>G
ENST00000254722.9:c.787-10C>G MANE Select ENSP00000254722.4:n.787-10C>G
NM_001329903.1:c.787-10C>G NP_001316832.1:n.787-10C>G
NM_001329903.2:c.787-10C>G NP_001316832.1:n.787-10C>G
NM_001329904.1:c.226-10C>G NP_001316833.1:n.226-10C>G
NM_001329904.2:c.226-10C>G NP_001316833.1:n.226-10C>G
NM_001329905.1:c.226-10C>G NP_001316834.1:n.226-10C>G
NM_001329905.2:c.226-10C>G NP_001316834.1:n.226-10C>G
NM_002615.5:c.787-10C>G NP_002606.3:n.787-10C>G
NM_002615.6:c.787-10C>G NP_002606.3:n.787-10C>G
ENST00000254722.8:c.787-10C>G ENSP00000254722.4:n.787-10C>G
ENST00000572048.1:c.226-10C>G ENSP00000458484.1:n.226-10C>G
ENST00000572517.1:n.73C>G
ENST00000573763.1:c.181-10C>G ENSP00000461405.1:n.181-10C>G
ENST00000576406.5:c.226-10C>G ENSP00000461214.1:n.226-10C>G