Canonical Allele Identifier: CA497287342

Gene: SERPINF1

Linked Data

• MyVariant Identifiers: chr17:g.1675284G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1771990G>C , CM000679.2:g.1771990G>C	GRCh38
NC_000017.10:g.1675284G>C , CM000679.1:g.1675284G>C	GRCh37
NC_000017.9:g.1622034G>C	NCBI36
NG_028180.1:g.15026G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.558G>C MANE Select	ENSP00000254722.4:p.Ala186=
ENST00000254722.8:c.558G>C	ENSP00000254722.4:p.Ala186=
ENST00000570820.1:n.778G>C
ENST00000572048.1:c.-4G>C	ENSP00000458484.1:n.-4G>C
ENST00000573763.1:c.-44G>C	ENSP00000461405.1:n.-44G>C
ENST00000576406.5:c.-4G>C	ENSP00000461214.1:n.-4G>C
NM_002615.5:c.558G>C	NP_002606.3:p.Ala186=
NM_001329903.1:c.558G>C	NP_001316832.1:p.Ala186=
NM_001329904.1:c.-4G>C	NP_001316833.1:n.-4G>C
NM_001329905.1:c.-4G>C	NP_001316834.1:n.-4G>C
NM_002615.6:c.558G>C	NP_002606.3:p.Ala186=
NM_002615.7:c.558G>C MANE Select	NP_002606.3:p.Ala186=
NM_001329903.2:c.558G>C	NP_001316832.1:p.Ala186=
NM_001329904.2:c.-4G>C	NP_001316833.1:n.-4G>C
NM_001329905.2:c.-4G>C	NP_001316834.1:n.-4G>C