Canonical Allele Identifier: CA1036160583

Gene: PROC

Linked Data

• dbSNP Id: rs910619185
• gnomAD v3: 2-127428960-A-C
• gnomAD v4: 2-127428960-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428960A>C , CM000664.2:g.127428960A>C	GRCh38
NC_000002.11:g.128186536A>C , CM000664.1:g.128186536A>C	GRCh37
NC_000002.10:g.127903006A>C	NCBI36
NG_016323.1:g.15541A>C , LRG_599:g.15541A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.*14A>C MANE Select	ENSP00000234071.4:n.*14A>C
ENST00000234071.7:c.*14A>C	ENSP00000234071.3:n.*14A>C
ENST00000402125.2:c.724A>C
ENST00000409048.1:c.*14A>C	ENSP00000386679.1:n.*14A>C
NM_000312.3:c.*14A>C , LRG_599t1:c.*14A>C	NP_000303.1:n.*14A>C
XM_005263715.3:c.*14A>C	XP_005263772.1:n.*14A>C
XM_005263716.3:c.*14A>C	XP_005263773.1:n.*14A>C
XM_005263717.3:c.*14A>C	XP_005263774.1:n.*14A>C
XR_923313.1:n.1332-696T>G
XM_005263717.4:c.*14A>C	XP_005263774.1:n.*14A>C
XM_017004505.1:c.*14A>C	XP_016859994.1:n.*14A>C
XM_024453002.1:c.*14A>C	XP_024308770.1:n.*14A>C
XM_024453003.1:c.*14A>C	XP_024308771.1:n.*14A>C
XM_024453004.1:c.*14A>C	XP_024308772.1:n.*14A>C
XM_024453005.1:c.*14A>C	XP_024308773.1:n.*14A>C
XM_024453006.1:c.*14A>C	XP_024308774.1:n.*14A>C
XR_001739705.1:n.3607-696T>G
XR_923313.2:n.4043-696T>G
NM_000312.4:c.*14A>C MANE Select	NP_000303.1:n.*14A>C
NM_001375602.1:c.*14A>C	NP_001362531.1:n.*14A>C
NM_001375603.1:c.*14A>C	NP_001362532.1:n.*14A>C
NM_001375604.1:c.*14A>C	NP_001362533.1:n.*14A>C
NM_001375605.1:c.*14A>C	NP_001362534.1:n.*14A>C
NM_001375606.1:c.*14A>C	NP_001362535.1:n.*14A>C
NM_001375607.1:c.*14A>C	NP_001362536.1:n.*14A>C
NM_001375608.1:c.*14A>C	NP_001362537.1:n.*14A>C
NM_001375609.1:c.*14A>C	NP_001362538.1:n.*14A>C
NM_001375610.1:c.*14A>C	NP_001362539.1:n.*14A>C
NM_001375611.1:c.*14A>C	NP_001362540.1:n.*14A>C
NM_001375613.1:c.*14A>C	NP_001362542.1:n.*14A>C