Canonical Allele Identifier: CA8274932
Community Standard Title: NM_002615.7(SERPINF1):c.998-1G>A
Gene: SERPINF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1777186G>A , CM000679.2:g.1777186G>A GRCh38
NC_000017.10:g.1680480G>A , CM000679.1:g.1680480G>A GRCh37
NC_000017.9:g.1627230G>A NCBI36
NG_028180.1:g.20222G>A

Transcript Alleles

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