Canonical Allele Identifier: CA434461647

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619667G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900823G>A , CM000665.2:g.93900823G>A	GRCh38
NC_000003.11:g.93619667G>A , CM000665.1:g.93619667G>A	GRCh37
NC_000003.10:g.95102357G>A	NCBI36
NG_009813.1:g.78268C>T , LRG_572:g.78268C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.708C>T	ENSP00000330021.7:p.Leu236=
ENST00000394236.9:c.708C>T MANE Select	ENSP00000377783.3:p.Leu236=
ENST00000407433.6:c.663C>T	ENSP00000385794.2:p.Leu221=
ENST00000647936.1:c.708C>T	ENSP00000496822.1:p.Leu236=
ENST00000648381.1:n.876C>T
ENST00000648853.1:c.666C>T	ENSP00000497262.1:p.Leu222=
ENST00000649103.1:c.807C>T	ENSP00000497962.1:n.807C>T
ENST00000650591.1:c.804C>T	ENSP00000497376.1:p.Leu268=
ENST00000394236.7:c.708C>T	ENSP00000377783.3:p.Leu236=
ENST00000407433.5:c.315C>T	ENSP00000385794.1:p.Leu105=
NM_000313.3:c.708C>T , LRG_572t1:c.708C>T	NP_000304.2:p.Leu236=
NM_001314077.1:c.804C>T , LRG_572t2:c.804C>T	NP_001301006.1:p.Leu268=
NM_000313.4:c.708C>T MANE Select	NP_000304.2:p.Leu236=
NM_001314077.2:c.804C>T	NP_001301006.1:p.Leu268=