Canonical Allele Identifier: CA348404590

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186014A>C (hg19) ; chr2:g.127428438A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428438A>C , CM000664.2:g.127428438A>C	GRCh38
NC_000002.11:g.128186014A>C , CM000664.1:g.128186014A>C	GRCh37
NC_000002.10:g.127902484A>C	NCBI36
NG_016323.1:g.15019A>C , LRG_599:g.15019A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.878A>C MANE Select	ENSP00000234071.4:p.Lys293Thr
ENST00000234071.7:c.878A>C	ENSP00000234071.3:p.Lys293Thr
ENST00000402125.2:c.202A>C
ENST00000409048.1:c.980A>C	ENSP00000386679.1:p.Lys327Thr
NM_000312.3:c.878A>C , LRG_599t1:c.878A>C	NP_000303.1:p.Lys293Thr
XM_005263715.3:c.1061A>C	XP_005263772.1:p.Lys354Thr
XM_005263716.3:c.1043A>C	XP_005263773.1:p.Lys348Thr
XM_005263717.3:c.941A>C	XP_005263774.1:p.Lys314Thr
XR_923313.1:n.1332-174T>G
XM_005263717.4:c.941A>C	XP_005263774.1:p.Lys314Thr
XM_017004505.1:c.1121A>C	XP_016859994.1:p.Lys374Thr
XM_024453002.1:c.1223A>C	XP_024308770.1:p.Lys408Thr
XM_024453003.1:c.1163A>C	XP_024308771.1:p.Lys388Thr
XM_024453004.1:c.1061A>C	XP_024308772.1:p.Lys354Thr
XM_024453005.1:c.1043A>C	XP_024308773.1:p.Lys348Thr
XM_024453006.1:c.980A>C	XP_024308774.1:p.Lys327Thr
XR_001739705.1:n.3607-174T>G
XR_923313.2:n.4043-174T>G
NM_000312.4:c.878A>C MANE Select	NP_000303.1:p.Lys293Thr
NM_001375602.1:c.1061A>C	NP_001362531.1:p.Lys354Thr
NM_001375603.1:c.1043A>C	NP_001362532.1:p.Lys348Thr
NM_001375604.1:c.941A>C	NP_001362533.1:p.Lys314Thr
NM_001375605.1:c.980A>C	NP_001362534.1:p.Lys327Thr
NM_001375606.1:c.1046A>C	NP_001362535.1:p.Lys349Thr
NM_001375607.1:c.1064A>C	NP_001362536.1:p.Lys355Thr
NM_001375608.1:c.821A>C	NP_001362537.1:p.Lys274Thr
NM_001375609.1:c.854A>C	NP_001362538.1:p.Lys285Thr
NM_001375610.1:c.872A>C	NP_001362539.1:p.Lys291Thr
NM_001375611.1:c.878A>C	NP_001362540.1:p.Lys293Thr
NM_001375613.1:c.878A>C	NP_001362542.1:p.Lys293Thr