Canonical Allele Identifier: CA2752102968

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428340T>C , CM000664.2:g.127428340T>C	GRCh38
NC_000002.11:g.128185916T>C , CM000664.1:g.128185916T>C	GRCh37
NC_000002.10:g.127902386T>C	NCBI36
NG_016323.1:g.14921T>C , LRG_599:g.14921T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.797-17T>C MANE Select	ENSP00000234071.4:n.797-17T>C
ENST00000234071.7:c.797-17T>C	ENSP00000234071.3:n.797-17T>C
ENST00000402125.2:c.121-17T>C
ENST00000409048.1:c.899-17T>C	ENSP00000386679.1:n.899-17T>C
NM_000312.3:c.797-17T>C , LRG_599t1:c.797-17T>C	NP_000303.1:n.797-17T>C
XM_005263715.3:c.980-17T>C	XP_005263772.1:n.980-17T>C
XM_005263716.3:c.962-17T>C	XP_005263773.1:n.962-17T>C
XM_005263717.3:c.860-17T>C	XP_005263774.1:n.860-17T>C
XR_923313.1:n.1332-76A>G
XM_005263717.4:c.860-17T>C	XP_005263774.1:n.860-17T>C
XM_017004505.1:c.1040-17T>C	XP_016859994.1:n.1040-17T>C
XM_024453002.1:c.1142-17T>C	XP_024308770.1:n.1142-17T>C
XM_024453003.1:c.1082-17T>C	XP_024308771.1:n.1082-17T>C
XM_024453004.1:c.980-17T>C	XP_024308772.1:n.980-17T>C
XM_024453005.1:c.962-17T>C	XP_024308773.1:n.962-17T>C
XM_024453006.1:c.899-17T>C	XP_024308774.1:n.899-17T>C
XR_001739705.1:n.3607-76A>G
XR_923313.2:n.4043-76A>G
NM_000312.4:c.797-17T>C MANE Select	NP_000303.1:n.797-17T>C
NM_001375602.1:c.980-17T>C	NP_001362531.1:n.980-17T>C
NM_001375603.1:c.962-17T>C	NP_001362532.1:n.962-17T>C
NM_001375604.1:c.860-17T>C	NP_001362533.1:n.860-17T>C
NM_001375605.1:c.899-17T>C	NP_001362534.1:n.899-17T>C
NM_001375606.1:c.965-17T>C	NP_001362535.1:n.965-17T>C
NM_001375607.1:c.983-17T>C	NP_001362536.1:n.983-17T>C
NM_001375608.1:c.740-17T>C	NP_001362537.1:n.740-17T>C
NM_001375609.1:c.773-17T>C	NP_001362538.1:n.773-17T>C
NM_001375610.1:c.791-17T>C	NP_001362539.1:n.791-17T>C
NM_001375611.1:c.797-17T>C	NP_001362540.1:n.797-17T>C
NM_001375613.1:c.797-17T>C	NP_001362542.1:n.797-17T>C