Canonical Allele Identifier: CA348405712

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186214C>G (hg19) ; chr2:g.127428638C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428638C>G , CM000664.2:g.127428638C>G	GRCh38
NC_000002.11:g.128186214C>G , CM000664.1:g.128186214C>G	GRCh37
NC_000002.10:g.127902684C>G	NCBI36
NG_016323.1:g.15219C>G , LRG_599:g.15219C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1078C>G MANE Select	ENSP00000234071.4:p.Leu360Val
ENST00000234071.7:c.1078C>G	ENSP00000234071.3:p.Leu360Val
ENST00000402125.2:c.402C>G
ENST00000409048.1:c.1180C>G	ENSP00000386679.1:p.Leu394Val
NM_000312.3:c.1078C>G , LRG_599t1:c.1078C>G	NP_000303.1:p.Leu360Val
XM_005263715.3:c.1261C>G	XP_005263772.1:p.Leu421Val
XM_005263716.3:c.1243C>G	XP_005263773.1:p.Leu415Val
XM_005263717.3:c.1141C>G	XP_005263774.1:p.Leu381Val
XR_923313.1:n.1332-374G>C
XM_005263717.4:c.1141C>G	XP_005263774.1:p.Leu381Val
XM_017004505.1:c.1321C>G	XP_016859994.1:p.Leu441Val
XM_024453002.1:c.1423C>G	XP_024308770.1:p.Leu475Val
XM_024453003.1:c.1363C>G	XP_024308771.1:p.Leu455Val
XM_024453004.1:c.1261C>G	XP_024308772.1:p.Leu421Val
XM_024453005.1:c.1243C>G	XP_024308773.1:p.Leu415Val
XM_024453006.1:c.1180C>G	XP_024308774.1:p.Leu394Val
XR_001739705.1:n.3607-374G>C
XR_923313.2:n.4043-374G>C
NM_000312.4:c.1078C>G MANE Select	NP_000303.1:p.Leu360Val
NM_001375602.1:c.1261C>G	NP_001362531.1:p.Leu421Val
NM_001375603.1:c.1243C>G	NP_001362532.1:p.Leu415Val
NM_001375604.1:c.1141C>G	NP_001362533.1:p.Leu381Val
NM_001375605.1:c.1180C>G	NP_001362534.1:p.Leu394Val
NM_001375606.1:c.1246C>G	NP_001362535.1:p.Leu416Val
NM_001375607.1:c.1264C>G	NP_001362536.1:p.Leu422Val
NM_001375608.1:c.1021C>G	NP_001362537.1:p.Leu341Val
NM_001375609.1:c.1054C>G	NP_001362538.1:p.Leu352Val
NM_001375610.1:c.1072C>G	NP_001362539.1:p.Leu358Val
NM_001375611.1:c.1078C>G	NP_001362540.1:p.Leu360Val
NM_001375613.1:c.1078C>G	NP_001362542.1:p.Leu360Val