Canonical Allele Identifier: CA2586969908

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428453del , CM000664.2:g.127428453del	GRCh38
NC_000002.11:g.128186029del , CM000664.1:g.128186029del	GRCh37
NC_000002.10:g.127902499del	NCBI36
NG_016323.1:g.15034del , LRG_599:g.15034del

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.893del MANE Select	ENSP00000234071.4:p.Asn298MetfsTer18
ENST00000234071.7:c.893del	ENSP00000234071.3:p.Asn298MetfsTer18
ENST00000402125.2:c.217del
ENST00000409048.1:c.995del	ENSP00000386679.1:p.Asn332MetfsTer18
NM_000312.3:c.893del , LRG_599t1:c.893del	NP_000303.1:p.Asn298MetfsTer18
XM_005263715.3:c.1076del	XP_005263772.1:p.Asn359MetfsTer18
XM_005263716.3:c.1058del	XP_005263773.1:p.Asn353MetfsTer18
XM_005263717.3:c.956del	XP_005263774.1:p.Asn319MetfsTer18
XR_923313.1:n.1332-188del
XM_005263717.4:c.956del	XP_005263774.1:p.Asn319MetfsTer18
XM_017004505.1:c.1136del	XP_016859994.1:p.Asn379MetfsTer18
XM_024453002.1:c.1238del	XP_024308770.1:p.Asn413MetfsTer18
XM_024453003.1:c.1178del	XP_024308771.1:p.Asn393MetfsTer18
XM_024453004.1:c.1076del	XP_024308772.1:p.Asn359MetfsTer18
XM_024453005.1:c.1058del	XP_024308773.1:p.Asn353MetfsTer18
XM_024453006.1:c.995del	XP_024308774.1:p.Asn332MetfsTer18
XR_001739705.1:n.3607-188del
XR_923313.2:n.4043-188del
NM_000312.4:c.893del MANE Select	NP_000303.1:p.Asn298MetfsTer18
NM_001375602.1:c.1076del	NP_001362531.1:p.Asn359MetfsTer18
NM_001375603.1:c.1058del	NP_001362532.1:p.Asn353MetfsTer18
NM_001375604.1:c.956del	NP_001362533.1:p.Asn319MetfsTer18
NM_001375605.1:c.995del	NP_001362534.1:p.Asn332MetfsTer18
NM_001375606.1:c.1061del	NP_001362535.1:p.Asn354MetfsTer18
NM_001375607.1:c.1079del	NP_001362536.1:p.Asn360MetfsTer18
NM_001375608.1:c.836del	NP_001362537.1:p.Asn279MetfsTer18
NM_001375609.1:c.869del	NP_001362538.1:p.Asn290MetfsTer18
NM_001375610.1:c.887del	NP_001362539.1:p.Asn296MetfsTer18
NM_001375611.1:c.893del	NP_001362540.1:p.Asn298MetfsTer18
NM_001375613.1:c.893del	NP_001362542.1:p.Asn298MetfsTer18