Canonical Allele Identifier: CA1286884376

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428241_127428242delinsCT , CM000664.2:g.127428241_127428242delinsCT	GRCh38
NC_000002.11:g.128185817_128185818delinsCT , CM000664.1:g.128185817_128185818delinsCT	GRCh37
NC_000002.10:g.127902287_127902288delinsCT	NCBI36
NG_016323.1:g.14822_14823delinsCT , LRG_599:g.14822_14823delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.797-116_797-115delinsCT MANE Select	ENSP00000234071.4:n.797-116_797-115delinsCT
ENST00000234071.7:c.797-116_797-115delinsCT	ENSP00000234071.3:n.797-116_797-115delinsCT
ENST00000402125.2:c.121-116_121-115delinsCT
ENST00000409048.1:c.899-116_899-115delinsCT	ENSP00000386679.1:n.899-116_899-115delinsCT
NM_000312.3:c.797-116_797-115delinsCT , LRG_599t1:c.797-116_797-115delinsCT	NP_000303.1:n.797-116_797-115delinsCT
XM_005263715.3:c.980-116_980-115delinsCT	XP_005263772.1:n.980-116_980-115delinsCT
XM_005263716.3:c.962-116_962-115delinsCT	XP_005263773.1:n.962-116_962-115delinsCT
XM_005263717.3:c.860-116_860-115delinsCT	XP_005263774.1:n.860-116_860-115delinsCT
XR_923313.1:n.1354_1355delinsAG
XM_005263717.4:c.860-116_860-115delinsCT	XP_005263774.1:n.860-116_860-115delinsCT
XM_017004505.1:c.1040-116_1040-115delinsCT	XP_016859994.1:n.1040-116_1040-115delinsCT
XM_024453002.1:c.1142-116_1142-115delinsCT	XP_024308770.1:n.1142-116_1142-115delinsCT
XM_024453003.1:c.1082-116_1082-115delinsCT	XP_024308771.1:n.1082-116_1082-115delinsCT
XM_024453004.1:c.980-116_980-115delinsCT	XP_024308772.1:n.980-116_980-115delinsCT
XM_024453005.1:c.962-116_962-115delinsCT	XP_024308773.1:n.962-116_962-115delinsCT
XM_024453006.1:c.899-116_899-115delinsCT	XP_024308774.1:n.899-116_899-115delinsCT
XR_001739705.1:n.3629_3630delinsAG
XR_923313.2:n.4065_4066delinsAG
NM_000312.4:c.797-116_797-115delinsCT MANE Select	NP_000303.1:n.797-116_797-115delinsCT
NM_001375602.1:c.980-116_980-115delinsCT	NP_001362531.1:n.980-116_980-115delinsCT
NM_001375603.1:c.962-116_962-115delinsCT	NP_001362532.1:n.962-116_962-115delinsCT
NM_001375604.1:c.860-116_860-115delinsCT	NP_001362533.1:n.860-116_860-115delinsCT
NM_001375605.1:c.899-116_899-115delinsCT	NP_001362534.1:n.899-116_899-115delinsCT
NM_001375606.1:c.965-116_965-115delinsCT	NP_001362535.1:n.965-116_965-115delinsCT
NM_001375607.1:c.983-116_983-115delinsCT	NP_001362536.1:n.983-116_983-115delinsCT
NM_001375608.1:c.740-116_740-115delinsCT	NP_001362537.1:n.740-116_740-115delinsCT
NM_001375609.1:c.773-116_773-115delinsCT	NP_001362538.1:n.773-116_773-115delinsCT
NM_001375610.1:c.791-116_791-115delinsCT	NP_001362539.1:n.791-116_791-115delinsCT
NM_001375611.1:c.797-116_797-115delinsCT	NP_001362540.1:n.797-116_797-115delinsCT
NM_001375613.1:c.797-116_797-115delinsCT	NP_001362542.1:n.797-116_797-115delinsCT