Canonical Allele Identifier: CA1385030684

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879383_93879385delinsAAC , CM000665.2:g.93879383_93879385delinsAAC	GRCh38
NC_000003.11:g.93598227_93598229delinsAAC , CM000665.1:g.93598227_93598229delinsAAC	GRCh37
NC_000003.10:g.95080917_95080919delinsAAC	NCBI36
NG_009813.1:g.99706_99708delinsGTT , LRG_572:g.99706_99708delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1493-71_1493-69delinsGTT	ENSP00000330021.7:n.1493-71_1493-69delinsGTT
ENST00000394236.9:c.1493-71_1493-69delinsGTT MANE Select	ENSP00000377783.3:n.1493-71_1493-69delinsGTT
ENST00000407433.6:c.1448-71_1448-69delinsGTT	ENSP00000385794.2:n.1448-71_1448-69delinsGTT
ENST00000647936.1:c.1493-71_1493-69delinsGTT	ENSP00000496822.1:n.1493-71_1493-69delinsGTT
ENST00000648381.1:n.1661-71_1661-69delinsGTT
ENST00000648853.1:c.1451-71_1451-69delinsGTT	ENSP00000497262.1:n.1451-71_1451-69delinsGTT
ENST00000649103.1:c.1592-71_1592-69delinsGTT	ENSP00000497962.1:n.1592-71_1592-69delinsGTT
ENST00000649585.1:c.436-71_436-69delinsGTT	ENSP00000498163.1:n.436-71_436-69delinsGTT
ENST00000650591.1:c.1589-71_1589-69delinsGTT	ENSP00000497376.1:n.1589-71_1589-69delinsGTT
ENST00000394236.7:c.1493-71_1493-69delinsGTT	ENSP00000377783.3:n.1493-71_1493-69delinsGTT
ENST00000407433.5:c.1100-71_1100-69delinsGTT	ENSP00000385794.1:n.1100-71_1100-69delinsGTT
NM_000313.3:c.1493-71_1493-69delinsGTT , LRG_572t1:c.1493-71_1493-69delinsGTT	NP_000304.2:n.1493-71_1493-69delinsGTT
NM_001314077.1:c.1589-71_1589-69delinsGTT , LRG_572t2:c.1589-71_1589-69delinsGTT	NP_001301006.1:n.1589-71_1589-69delinsGTT
NM_000313.4:c.1493-71_1493-69delinsGTT MANE Select	NP_000304.2:n.1493-71_1493-69delinsGTT
NM_001314077.2:c.1589-71_1589-69delinsGTT	NP_001301006.1:n.1589-71_1589-69delinsGTT