Canonical Allele Identifier: CA348405672

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186194A>T (hg19) ; chr2:g.127428618A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428618A>T , CM000664.2:g.127428618A>T	GRCh38
NC_000002.11:g.128186194A>T , CM000664.1:g.128186194A>T	GRCh37
NC_000002.10:g.127902664A>T	NCBI36
NG_016323.1:g.15199A>T , LRG_599:g.15199A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1058A>T MANE Select	ENSP00000234071.4:p.Lys353Met
ENST00000234071.7:c.1058A>T	ENSP00000234071.3:p.Lys353Met
ENST00000402125.2:c.382A>T
ENST00000409048.1:c.1160A>T	ENSP00000386679.1:p.Lys387Met
NM_000312.3:c.1058A>T , LRG_599t1:c.1058A>T	NP_000303.1:p.Lys353Met
XM_005263715.3:c.1241A>T	XP_005263772.1:p.Lys414Met
XM_005263716.3:c.1223A>T	XP_005263773.1:p.Lys408Met
XM_005263717.3:c.1121A>T	XP_005263774.1:p.Lys374Met
XR_923313.1:n.1332-354T>A
XM_005263717.4:c.1121A>T	XP_005263774.1:p.Lys374Met
XM_017004505.1:c.1301A>T	XP_016859994.1:p.Lys434Met
XM_024453002.1:c.1403A>T	XP_024308770.1:p.Lys468Met
XM_024453003.1:c.1343A>T	XP_024308771.1:p.Lys448Met
XM_024453004.1:c.1241A>T	XP_024308772.1:p.Lys414Met
XM_024453005.1:c.1223A>T	XP_024308773.1:p.Lys408Met
XM_024453006.1:c.1160A>T	XP_024308774.1:p.Lys387Met
XR_001739705.1:n.3607-354T>A
XR_923313.2:n.4043-354T>A
NM_000312.4:c.1058A>T MANE Select	NP_000303.1:p.Lys353Met
NM_001375602.1:c.1241A>T	NP_001362531.1:p.Lys414Met
NM_001375603.1:c.1223A>T	NP_001362532.1:p.Lys408Met
NM_001375604.1:c.1121A>T	NP_001362533.1:p.Lys374Met
NM_001375605.1:c.1160A>T	NP_001362534.1:p.Lys387Met
NM_001375606.1:c.1226A>T	NP_001362535.1:p.Lys409Met
NM_001375607.1:c.1244A>T	NP_001362536.1:p.Lys415Met
NM_001375608.1:c.1001A>T	NP_001362537.1:p.Lys334Met
NM_001375609.1:c.1034A>T	NP_001362538.1:p.Lys345Met
NM_001375610.1:c.1052A>T	NP_001362539.1:p.Lys351Met
NM_001375611.1:c.1058A>T	NP_001362540.1:p.Lys353Met
NM_001375613.1:c.1058A>T	NP_001362542.1:p.Lys353Met