Canonical Allele Identifier: CA348406587

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186424C>G (hg19) ; chr2:g.127428848C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428848C>G , CM000664.2:g.127428848C>G	GRCh38
NC_000002.11:g.128186424C>G , CM000664.1:g.128186424C>G	GRCh37
NC_000002.10:g.127902894C>G	NCBI36
NG_016323.1:g.15429C>G , LRG_599:g.15429C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1288C>G MANE Select	ENSP00000234071.4:p.His430Asp
ENST00000234071.7:c.1288C>G	ENSP00000234071.3:p.His430Asp
ENST00000402125.2:c.612C>G
ENST00000409048.1:c.1390C>G	ENSP00000386679.1:p.His464Asp
NM_000312.3:c.1288C>G , LRG_599t1:c.1288C>G	NP_000303.1:p.His430Asp
XM_005263715.3:c.1471C>G	XP_005263772.1:p.His491Asp
XM_005263716.3:c.1453C>G	XP_005263773.1:p.His485Asp
XM_005263717.3:c.1351C>G	XP_005263774.1:p.His451Asp
XR_923313.1:n.1332-584G>C
XM_005263717.4:c.1351C>G	XP_005263774.1:p.His451Asp
XM_017004505.1:c.1531C>G	XP_016859994.1:p.His511Asp
XM_024453002.1:c.1633C>G	XP_024308770.1:p.His545Asp
XM_024453003.1:c.1573C>G	XP_024308771.1:p.His525Asp
XM_024453004.1:c.1471C>G	XP_024308772.1:p.His491Asp
XM_024453005.1:c.1453C>G	XP_024308773.1:p.His485Asp
XM_024453006.1:c.1390C>G	XP_024308774.1:p.His464Asp
XR_001739705.1:n.3607-584G>C
XR_923313.2:n.4043-584G>C
NM_000312.4:c.1288C>G MANE Select	NP_000303.1:p.His430Asp
NM_001375602.1:c.1471C>G	NP_001362531.1:p.His491Asp
NM_001375603.1:c.1453C>G	NP_001362532.1:p.His485Asp
NM_001375604.1:c.1351C>G	NP_001362533.1:p.His451Asp
NM_001375605.1:c.1390C>G	NP_001362534.1:p.His464Asp
NM_001375606.1:c.1456C>G	NP_001362535.1:p.His486Asp
NM_001375607.1:c.1474C>G	NP_001362536.1:p.His492Asp
NM_001375608.1:c.1231C>G	NP_001362537.1:p.His411Asp
NM_001375609.1:c.1264C>G	NP_001362538.1:p.His422Asp
NM_001375610.1:c.1282C>G	NP_001362539.1:p.His428Asp
NM_001375611.1:c.1288C>G	NP_001362540.1:p.His430Asp
NM_001375613.1:c.1288C>G	NP_001362542.1:p.His430Asp