Canonical Allele Identifier: CA428871675

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186099G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428523G>T , CM000664.2:g.127428523G>T	GRCh38
NC_000002.11:g.128186099G>T , CM000664.1:g.128186099G>T	GRCh37
NC_000002.10:g.127902569G>T	NCBI36
NG_016323.1:g.15104G>T , LRG_599:g.15104G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.963G>T MANE Select	ENSP00000234071.4:p.Pro321=
ENST00000234071.7:c.963G>T	ENSP00000234071.3:p.Pro321=
ENST00000402125.2:c.287G>T
ENST00000409048.1:c.1065G>T	ENSP00000386679.1:p.Pro355=
NM_000312.3:c.963G>T , LRG_599t1:c.963G>T	NP_000303.1:p.Pro321=
XM_005263715.3:c.1146G>T	XP_005263772.1:p.Pro382=
XM_005263716.3:c.1128G>T	XP_005263773.1:p.Pro376=
XM_005263717.3:c.1026G>T	XP_005263774.1:p.Pro342=
XR_923313.1:n.1332-259C>A
XM_005263717.4:c.1026G>T	XP_005263774.1:p.Pro342=
XM_017004505.1:c.1206G>T	XP_016859994.1:p.Pro402=
XM_024453002.1:c.1308G>T	XP_024308770.1:p.Pro436=
XM_024453003.1:c.1248G>T	XP_024308771.1:p.Pro416=
XM_024453004.1:c.1146G>T	XP_024308772.1:p.Pro382=
XM_024453005.1:c.1128G>T	XP_024308773.1:p.Pro376=
XM_024453006.1:c.1065G>T	XP_024308774.1:p.Pro355=
XR_001739705.1:n.3607-259C>A
XR_923313.2:n.4043-259C>A
NM_000312.4:c.963G>T MANE Select	NP_000303.1:p.Pro321=
NM_001375602.1:c.1146G>T	NP_001362531.1:p.Pro382=
NM_001375603.1:c.1128G>T	NP_001362532.1:p.Pro376=
NM_001375604.1:c.1026G>T	NP_001362533.1:p.Pro342=
NM_001375605.1:c.1065G>T	NP_001362534.1:p.Pro355=
NM_001375606.1:c.1131G>T	NP_001362535.1:p.Pro377=
NM_001375607.1:c.1149G>T	NP_001362536.1:p.Pro383=
NM_001375608.1:c.906G>T	NP_001362537.1:p.Pro302=
NM_001375609.1:c.939G>T	NP_001362538.1:p.Pro313=
NM_001375610.1:c.957G>T	NP_001362539.1:p.Pro319=
NM_001375611.1:c.963G>T	NP_001362540.1:p.Pro321=
NM_001375613.1:c.963G>T	NP_001362542.1:p.Pro321=