Canonical Allele Identifier: CA348405711

Gene: PROC

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1078C>A MANE Select	ENSP00000234071.4:p.Leu360Ile
ENST00000234071.7:c.1078C>A	ENSP00000234071.3:p.Leu360Ile
ENST00000402125.2:c.402C>A
ENST00000409048.1:c.1180C>A	ENSP00000386679.1:p.Leu394Ile
NM_000312.3:c.1078C>A , LRG_599t1:c.1078C>A	NP_000303.1:p.Leu360Ile
XM_005263715.3:c.1261C>A	XP_005263772.1:p.Leu421Ile
XM_005263716.3:c.1243C>A	XP_005263773.1:p.Leu415Ile
XM_005263717.3:c.1141C>A	XP_005263774.1:p.Leu381Ile
XR_923313.1:n.1332-374G>T
XM_005263717.4:c.1141C>A	XP_005263774.1:p.Leu381Ile
XM_017004505.1:c.1321C>A	XP_016859994.1:p.Leu441Ile
XM_024453002.1:c.1423C>A	XP_024308770.1:p.Leu475Ile
XM_024453003.1:c.1363C>A	XP_024308771.1:p.Leu455Ile
XM_024453004.1:c.1261C>A	XP_024308772.1:p.Leu421Ile
XM_024453005.1:c.1243C>A	XP_024308773.1:p.Leu415Ile
XM_024453006.1:c.1180C>A	XP_024308774.1:p.Leu394Ile
XR_001739705.1:n.3607-374G>T
XR_923313.2:n.4043-374G>T
NM_000312.4:c.1078C>A MANE Select	NP_000303.1:p.Leu360Ile
NM_001375602.1:c.1261C>A	NP_001362531.1:p.Leu421Ile
NM_001375603.1:c.1243C>A	NP_001362532.1:p.Leu415Ile
NM_001375604.1:c.1141C>A	NP_001362533.1:p.Leu381Ile
NM_001375605.1:c.1180C>A	NP_001362534.1:p.Leu394Ile
NM_001375606.1:c.1246C>A	NP_001362535.1:p.Leu416Ile
NM_001375607.1:c.1264C>A	NP_001362536.1:p.Leu422Ile
NM_001375608.1:c.1021C>A	NP_001362537.1:p.Leu341Ile
NM_001375609.1:c.1054C>A	NP_001362538.1:p.Leu352Ile
NM_001375610.1:c.1072C>A	NP_001362539.1:p.Leu358Ile
NM_001375611.1:c.1078C>A	NP_001362540.1:p.Leu360Ile
NM_001375613.1:c.1078C>A	NP_001362542.1:p.Leu360Ile