Canonical Allele Identifier: CA348404282

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128185951G>C (hg19) ; chr2:g.127428375G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428375G>C , CM000664.2:g.127428375G>C	GRCh38
NC_000002.11:g.128185951G>C , CM000664.1:g.128185951G>C	GRCh37
NC_000002.10:g.127902421G>C	NCBI36
NG_016323.1:g.14956G>C , LRG_599:g.14956G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.815G>C MANE Select	ENSP00000234071.4:p.Arg272Pro
ENST00000234071.7:c.815G>C	ENSP00000234071.3:p.Arg272Pro
ENST00000402125.2:c.139G>C
ENST00000409048.1:c.917G>C	ENSP00000386679.1:p.Arg306Pro
NM_000312.3:c.815G>C , LRG_599t1:c.815G>C	NP_000303.1:p.Arg272Pro
XM_005263715.3:c.998G>C	XP_005263772.1:p.Arg333Pro
XM_005263716.3:c.980G>C	XP_005263773.1:p.Arg327Pro
XM_005263717.3:c.878G>C	XP_005263774.1:p.Arg293Pro
XR_923313.1:n.1332-111C>G
XM_005263717.4:c.878G>C	XP_005263774.1:p.Arg293Pro
XM_017004505.1:c.1058G>C	XP_016859994.1:p.Arg353Pro
XM_024453002.1:c.1160G>C	XP_024308770.1:p.Arg387Pro
XM_024453003.1:c.1100G>C	XP_024308771.1:p.Arg367Pro
XM_024453004.1:c.998G>C	XP_024308772.1:p.Arg333Pro
XM_024453005.1:c.980G>C	XP_024308773.1:p.Arg327Pro
XM_024453006.1:c.917G>C	XP_024308774.1:p.Arg306Pro
XR_001739705.1:n.3607-111C>G
XR_923313.2:n.4043-111C>G
NM_000312.4:c.815G>C MANE Select	NP_000303.1:p.Arg272Pro
NM_001375602.1:c.998G>C	NP_001362531.1:p.Arg333Pro
NM_001375603.1:c.980G>C	NP_001362532.1:p.Arg327Pro
NM_001375604.1:c.878G>C	NP_001362533.1:p.Arg293Pro
NM_001375605.1:c.917G>C	NP_001362534.1:p.Arg306Pro
NM_001375606.1:c.983G>C	NP_001362535.1:p.Arg328Pro
NM_001375607.1:c.1001G>C	NP_001362536.1:p.Arg334Pro
NM_001375608.1:c.758G>C	NP_001362537.1:p.Arg253Pro
NM_001375609.1:c.791G>C	NP_001362538.1:p.Arg264Pro
NM_001375610.1:c.809G>C	NP_001362539.1:p.Arg270Pro
NM_001375611.1:c.815G>C	NP_001362540.1:p.Arg272Pro
NM_001375613.1:c.815G>C	NP_001362542.1:p.Arg272Pro