Canonical Allele Identifier: CA348405012

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186085C>A (hg19) ; chr2:g.127428509C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428509C>A , CM000664.2:g.127428509C>A	GRCh38
NC_000002.11:g.128186085C>A , CM000664.1:g.128186085C>A	GRCh37
NC_000002.10:g.127902555C>A	NCBI36
NG_016323.1:g.15090C>A , LRG_599:g.15090C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.949C>A MANE Select	ENSP00000234071.4:p.Pro317Thr
ENST00000234071.7:c.949C>A	ENSP00000234071.3:p.Pro317Thr
ENST00000402125.2:c.273C>A
ENST00000409048.1:c.1051C>A	ENSP00000386679.1:p.Pro351Thr
NM_000312.3:c.949C>A , LRG_599t1:c.949C>A	NP_000303.1:p.Pro317Thr
XM_005263715.3:c.1132C>A	XP_005263772.1:p.Pro378Thr
XM_005263716.3:c.1114C>A	XP_005263773.1:p.Pro372Thr
XM_005263717.3:c.1012C>A	XP_005263774.1:p.Pro338Thr
XR_923313.1:n.1332-245G>T
XM_005263717.4:c.1012C>A	XP_005263774.1:p.Pro338Thr
XM_017004505.1:c.1192C>A	XP_016859994.1:p.Pro398Thr
XM_024453002.1:c.1294C>A	XP_024308770.1:p.Pro432Thr
XM_024453003.1:c.1234C>A	XP_024308771.1:p.Pro412Thr
XM_024453004.1:c.1132C>A	XP_024308772.1:p.Pro378Thr
XM_024453005.1:c.1114C>A	XP_024308773.1:p.Pro372Thr
XM_024453006.1:c.1051C>A	XP_024308774.1:p.Pro351Thr
XR_001739705.1:n.3607-245G>T
XR_923313.2:n.4043-245G>T
NM_000312.4:c.949C>A MANE Select	NP_000303.1:p.Pro317Thr
NM_001375602.1:c.1132C>A	NP_001362531.1:p.Pro378Thr
NM_001375603.1:c.1114C>A	NP_001362532.1:p.Pro372Thr
NM_001375604.1:c.1012C>A	NP_001362533.1:p.Pro338Thr
NM_001375605.1:c.1051C>A	NP_001362534.1:p.Pro351Thr
NM_001375606.1:c.1117C>A	NP_001362535.1:p.Pro373Thr
NM_001375607.1:c.1135C>A	NP_001362536.1:p.Pro379Thr
NM_001375608.1:c.892C>A	NP_001362537.1:p.Pro298Thr
NM_001375609.1:c.925C>A	NP_001362538.1:p.Pro309Thr
NM_001375610.1:c.943C>A	NP_001362539.1:p.Pro315Thr
NM_001375611.1:c.949C>A	NP_001362540.1:p.Pro317Thr
NM_001375613.1:c.949C>A	NP_001362542.1:p.Pro317Thr