Canonical Allele Identifier: CA428618858

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128185949G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428373G>T , CM000664.2:g.127428373G>T	GRCh38
NC_000002.11:g.128185949G>T , CM000664.1:g.128185949G>T	GRCh37
NC_000002.10:g.127902419G>T	NCBI36
NG_016323.1:g.14954G>T , LRG_599:g.14954G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.813G>T MANE Select	ENSP00000234071.4:p.Arg271=
ENST00000234071.7:c.813G>T	ENSP00000234071.3:p.Arg271=
ENST00000402125.2:c.137G>T
ENST00000409048.1:c.915G>T	ENSP00000386679.1:p.Arg305=
NM_000312.3:c.813G>T , LRG_599t1:c.813G>T	NP_000303.1:p.Arg271=
XM_005263715.3:c.996G>T	XP_005263772.1:p.Arg332=
XM_005263716.3:c.978G>T	XP_005263773.1:p.Arg326=
XM_005263717.3:c.876G>T	XP_005263774.1:p.Arg292=
XR_923313.1:n.1332-109C>A
XM_005263717.4:c.876G>T	XP_005263774.1:p.Arg292=
XM_017004505.1:c.1056G>T	XP_016859994.1:p.Arg352=
XM_024453002.1:c.1158G>T	XP_024308770.1:p.Arg386=
XM_024453003.1:c.1098G>T	XP_024308771.1:p.Arg366=
XM_024453004.1:c.996G>T	XP_024308772.1:p.Arg332=
XM_024453005.1:c.978G>T	XP_024308773.1:p.Arg326=
XM_024453006.1:c.915G>T	XP_024308774.1:p.Arg305=
XR_001739705.1:n.3607-109C>A
XR_923313.2:n.4043-109C>A
NM_000312.4:c.813G>T MANE Select	NP_000303.1:p.Arg271=
NM_001375602.1:c.996G>T	NP_001362531.1:p.Arg332=
NM_001375603.1:c.978G>T	NP_001362532.1:p.Arg326=
NM_001375604.1:c.876G>T	NP_001362533.1:p.Arg292=
NM_001375605.1:c.915G>T	NP_001362534.1:p.Arg305=
NM_001375606.1:c.981G>T	NP_001362535.1:p.Arg327=
NM_001375607.1:c.999G>T	NP_001362536.1:p.Arg333=
NM_001375608.1:c.756G>T	NP_001362537.1:p.Arg252=
NM_001375609.1:c.789G>T	NP_001362538.1:p.Arg263=
NM_001375610.1:c.807G>T	NP_001362539.1:p.Arg269=
NM_001375611.1:c.813G>T	NP_001362540.1:p.Arg271=
NM_001375613.1:c.813G>T	NP_001362542.1:p.Arg271=