Canonical Allele Identifier: CA8274681
Community Standard Title: NM_002615.7(SERPINF1):c.439+7C>T
Gene: SERPINF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1771191C>T , CM000679.2:g.1771191C>T GRCh38
NC_000017.10:g.1674485C>T , CM000679.1:g.1674485C>T GRCh37
NC_000017.9:g.1621235C>T NCBI36
NG_028180.1:g.14227C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002615.7:c.439+7C>T MANE Select NP_002606.3:n.439+7C>T
ENST00000254722.9:c.439+7C>T MANE Select ENSP00000254722.4:n.439+7C>T
NM_001329903.1:c.439+7C>T NP_001316832.1:n.439+7C>T
NM_001329903.2:c.439+7C>T NP_001316832.1:n.439+7C>T
NM_001329904.1:c.-123+7C>T NP_001316833.1:n.-123+7C>T
NM_001329904.2:c.-123+7C>T NP_001316833.1:n.-123+7C>T
NM_002615.5:c.439+7C>T NP_002606.3:n.439+7C>T
NM_002615.6:c.439+7C>T NP_002606.3:n.439+7C>T
ENST00000254722.8:c.439+7C>T ENSP00000254722.4:n.439+7C>T
ENST00000570820.1:n.659+7C>T
ENST00000571870.5:n.680+7C>T
ENST00000573770.5:c.*289+7C>T ENSP00000459107.1:n.*289+7C>T
ENST00000576406.5:c.-123+7C>T ENSP00000461214.1:n.-123+7C>T