Canonical Allele Identifier: CA397575238
Gene: SERPINF2 HGNC NCBI

Linked Data

gnomAD v4: 17-1754298-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1754298C>T , CM000679.2:g.1754298C>T GRCh38
NC_000017.10:g.1657592C>T , CM000679.1:g.1657592C>T GRCh37
NC_000017.9:g.1604342C>T NCBI36
NG_013215.1:g.16463C>T , LRG_885:g.16463C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382061.5:c.1240C>T ENSP00000371493.4:p.Pro414Ser
ENST00000453066.6:c.1240C>T MANE Select ENSP00000402286.2:p.Pro414Ser
ENST00000324015.7:c.1240C>T ENSP00000321853.3:p.Pro414Ser
ENST00000382061.4:c.1240C>T ENSP00000371493.4:p.Pro414Ser
ENST00000450523.6:c.1048C>T ENSP00000403877.2:p.Pro350Ser
NM_000934.3:c.1240C>T , LRG_885t1:c.1240C>T NP_000925.2:p.Pro414Ser
NM_001165920.1:c.1240C>T NP_001159392.1:p.Pro414Ser
NM_001165921.1:c.1048C>T NP_001159393.1:p.Pro350Ser
XM_005256699.3:c.1345C>T XP_005256756.1:p.Pro449Ser
XM_005256700.3:c.1252C>T XP_005256757.1:p.Pro418Ser
XM_005256701.3:c.1288C>T XP_005256758.2:p.Pro430Ser
XM_005256703.3:c.1159C>T XP_005256760.1:p.Pro387Ser
XM_005256701.4:c.1288C>T XP_005256758.2:p.Pro430Ser
XM_017024765.1:c.1252C>T XP_016880254.1:p.Pro418Ser
XM_024450805.1:c.1252C>T XP_024306573.1:p.Pro418Ser
NM_000934.4:c.1240C>T MANE Select NP_000925.2:p.Pro414Ser
NM_001165921.2:c.1048C>T NP_001159393.1:p.Pro350Ser