Canonical Allele Identifier: CA353674668

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646213T>G (hg19) ; chr3:g.93927369T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927369T>G , CM000665.2:g.93927369T>G	GRCh38
NC_000003.11:g.93646213T>G , CM000665.1:g.93646213T>G	GRCh37
NC_000003.10:g.95128903T>G	NCBI36
NG_009813.1:g.51722A>C , LRG_572:g.51722A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.115A>C	ENSP00000330021.7:p.Lys39Gln
ENST00000394236.9:c.115A>C MANE Select	ENSP00000377783.3:p.Lys39Gln
ENST00000407433.6:c.115A>C	ENSP00000385794.2:p.Lys39Gln
ENST00000472684.2:c.-279A>C	ENSP00000419616.2:n.-279A>C
ENST00000647936.1:c.115A>C	ENSP00000496822.1:p.Lys39Gln
ENST00000648381.1:n.283A>C
ENST00000648853.1:c.73A>C	ENSP00000497262.1:p.Lys25Gln
ENST00000649103.1:c.94A>C	ENSP00000497962.1:p.Lys32Gln
ENST00000650591.1:c.211A>C	ENSP00000497376.1:p.Lys71Gln
ENST00000348974.4:c.211A>C	ENSP00000330021.6:p.Lys71Gln
ENST00000394236.7:c.115A>C	ENSP00000377783.3:p.Lys39Gln
ENST00000407433.5:c.-279A>C	ENSP00000385794.1:n.-279A>C
ENST00000472684.1:c.-279A>C	ENSP00000419616.1:n.-279A>C
NM_000313.3:c.115A>C , LRG_572t1:c.115A>C	NP_000304.2:p.Lys39Gln
NM_001314077.1:c.211A>C , LRG_572t2:c.211A>C	NP_001301006.1:p.Lys71Gln
NM_000313.4:c.115A>C MANE Select	NP_000304.2:p.Lys39Gln
NM_001314077.2:c.211A>C	NP_001301006.1:p.Lys71Gln