Canonical Allele Identifier: CA348405963

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186275T>A (hg19) ; chr2:g.127428699T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428699T>A , CM000664.2:g.127428699T>A	GRCh38
NC_000002.11:g.128186275T>A , CM000664.1:g.128186275T>A	GRCh37
NC_000002.10:g.127902745T>A	NCBI36
NG_016323.1:g.15280T>A , LRG_599:g.15280T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1139T>A MANE Select	ENSP00000234071.4:p.Met380Lys
ENST00000234071.7:c.1139T>A	ENSP00000234071.3:p.Met380Lys
ENST00000402125.2:c.463T>A
ENST00000409048.1:c.1241T>A	ENSP00000386679.1:p.Met414Lys
NM_000312.3:c.1139T>A , LRG_599t1:c.1139T>A	NP_000303.1:p.Met380Lys
XM_005263715.3:c.1322T>A	XP_005263772.1:p.Met441Lys
XM_005263716.3:c.1304T>A	XP_005263773.1:p.Met435Lys
XM_005263717.3:c.1202T>A	XP_005263774.1:p.Met401Lys
XR_923313.1:n.1332-435A>T
XM_005263717.4:c.1202T>A	XP_005263774.1:p.Met401Lys
XM_017004505.1:c.1382T>A	XP_016859994.1:p.Met461Lys
XM_024453002.1:c.1484T>A	XP_024308770.1:p.Met495Lys
XM_024453003.1:c.1424T>A	XP_024308771.1:p.Met475Lys
XM_024453004.1:c.1322T>A	XP_024308772.1:p.Met441Lys
XM_024453005.1:c.1304T>A	XP_024308773.1:p.Met435Lys
XM_024453006.1:c.1241T>A	XP_024308774.1:p.Met414Lys
XR_001739705.1:n.3607-435A>T
XR_923313.2:n.4043-435A>T
NM_000312.4:c.1139T>A MANE Select	NP_000303.1:p.Met380Lys
NM_001375602.1:c.1322T>A	NP_001362531.1:p.Met441Lys
NM_001375603.1:c.1304T>A	NP_001362532.1:p.Met435Lys
NM_001375604.1:c.1202T>A	NP_001362533.1:p.Met401Lys
NM_001375605.1:c.1241T>A	NP_001362534.1:p.Met414Lys
NM_001375606.1:c.1307T>A	NP_001362535.1:p.Met436Lys
NM_001375607.1:c.1325T>A	NP_001362536.1:p.Met442Lys
NM_001375608.1:c.1082T>A	NP_001362537.1:p.Met361Lys
NM_001375609.1:c.1115T>A	NP_001362538.1:p.Met372Lys
NM_001375610.1:c.1133T>A	NP_001362539.1:p.Met378Lys
NM_001375611.1:c.1139T>A	NP_001362540.1:p.Met380Lys
NM_001375613.1:c.1139T>A	NP_001362542.1:p.Met380Lys