Canonical Allele Identifier: CA2577828453

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905743C>G , CM000665.2:g.93905743C>G	GRCh38
NC_000003.11:g.93624587C>G , CM000665.1:g.93624587C>G	GRCh37
NC_000003.10:g.95107277C>G	NCBI36
NG_009813.1:g.73348G>C , LRG_572:g.73348G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.601+41G>C	ENSP00000330021.7:n.601+41G>C
ENST00000394236.9:c.601+41G>C MANE Select	ENSP00000377783.3:n.601+41G>C
ENST00000407433.6:c.556+86G>C	ENSP00000385794.2:n.556+86G>C
ENST00000647936.1:c.601+41G>C	ENSP00000496822.1:n.601+41G>C
ENST00000648381.1:n.769+41G>C
ENST00000648853.1:c.559+41G>C	ENSP00000497262.1:n.559+41G>C
ENST00000649103.1:c.700+41G>C	ENSP00000497962.1:n.700+41G>C
ENST00000650591.1:c.697+41G>C	ENSP00000497376.1:n.697+41G>C
ENST00000394236.7:c.601+41G>C	ENSP00000377783.3:n.601+41G>C
ENST00000407433.5:c.208+41G>C	ENSP00000385794.1:n.208+41G>C
NM_000313.3:c.601+41G>C , LRG_572t1:c.601+41G>C	NP_000304.2:n.601+41G>C
NM_001314077.1:c.697+41G>C , LRG_572t2:c.697+41G>C	NP_001301006.1:n.697+41G>C
NM_000313.4:c.601+41G>C MANE Select	NP_000304.2:n.601+41G>C
NM_001314077.2:c.697+41G>C	NP_001301006.1:n.697+41G>C