Canonical Allele Identifier: CA428873025

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186219C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428643C>T , CM000664.2:g.127428643C>T	GRCh38
NC_000002.11:g.128186219C>T , CM000664.1:g.128186219C>T	GRCh37
NC_000002.10:g.127902689C>T	NCBI36
NG_016323.1:g.15224C>T , LRG_599:g.15224C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1083C>T MANE Select	ENSP00000234071.4:p.Asn361=
ENST00000234071.7:c.1083C>T	ENSP00000234071.3:p.Asn361=
ENST00000402125.2:c.407C>T
ENST00000409048.1:c.1185C>T	ENSP00000386679.1:p.Asn395=
NM_000312.3:c.1083C>T , LRG_599t1:c.1083C>T	NP_000303.1:p.Asn361=
XM_005263715.3:c.1266C>T	XP_005263772.1:p.Asn422=
XM_005263716.3:c.1248C>T	XP_005263773.1:p.Asn416=
XM_005263717.3:c.1146C>T	XP_005263774.1:p.Asn382=
XR_923313.1:n.1332-379G>A
XM_005263717.4:c.1146C>T	XP_005263774.1:p.Asn382=
XM_017004505.1:c.1326C>T	XP_016859994.1:p.Asn442=
XM_024453002.1:c.1428C>T	XP_024308770.1:p.Asn476=
XM_024453003.1:c.1368C>T	XP_024308771.1:p.Asn456=
XM_024453004.1:c.1266C>T	XP_024308772.1:p.Asn422=
XM_024453005.1:c.1248C>T	XP_024308773.1:p.Asn416=
XM_024453006.1:c.1185C>T	XP_024308774.1:p.Asn395=
XR_001739705.1:n.3607-379G>A
XR_923313.2:n.4043-379G>A
NM_000312.4:c.1083C>T MANE Select	NP_000303.1:p.Asn361=
NM_001375602.1:c.1266C>T	NP_001362531.1:p.Asn422=
NM_001375603.1:c.1248C>T	NP_001362532.1:p.Asn416=
NM_001375604.1:c.1146C>T	NP_001362533.1:p.Asn382=
NM_001375605.1:c.1185C>T	NP_001362534.1:p.Asn395=
NM_001375606.1:c.1251C>T	NP_001362535.1:p.Asn417=
NM_001375607.1:c.1269C>T	NP_001362536.1:p.Asn423=
NM_001375608.1:c.1026C>T	NP_001362537.1:p.Asn342=
NM_001375609.1:c.1059C>T	NP_001362538.1:p.Asn353=
NM_001375610.1:c.1077C>T	NP_001362539.1:p.Asn359=
NM_001375611.1:c.1083C>T	NP_001362540.1:p.Asn361=
NM_001375613.1:c.1083C>T	NP_001362542.1:p.Asn361=