Canonical Allele Identifier: CA348405825

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186244C>A (hg19) ; chr2:g.127428668C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428668C>A , CM000664.2:g.127428668C>A	GRCh38
NC_000002.11:g.128186244C>A , CM000664.1:g.128186244C>A	GRCh37
NC_000002.10:g.127902714C>A	NCBI36
NG_016323.1:g.15249C>A , LRG_599:g.15249C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1108C>A MANE Select	ENSP00000234071.4:p.His370Asn
ENST00000234071.7:c.1108C>A	ENSP00000234071.3:p.His370Asn
ENST00000402125.2:c.432C>A
ENST00000409048.1:c.1210C>A	ENSP00000386679.1:p.His404Asn
NM_000312.3:c.1108C>A , LRG_599t1:c.1108C>A	NP_000303.1:p.His370Asn
XM_005263715.3:c.1291C>A	XP_005263772.1:p.His431Asn
XM_005263716.3:c.1273C>A	XP_005263773.1:p.His425Asn
XM_005263717.3:c.1171C>A	XP_005263774.1:p.His391Asn
XR_923313.1:n.1332-404G>T
XM_005263717.4:c.1171C>A	XP_005263774.1:p.His391Asn
XM_017004505.1:c.1351C>A	XP_016859994.1:p.His451Asn
XM_024453002.1:c.1453C>A	XP_024308770.1:p.His485Asn
XM_024453003.1:c.1393C>A	XP_024308771.1:p.His465Asn
XM_024453004.1:c.1291C>A	XP_024308772.1:p.His431Asn
XM_024453005.1:c.1273C>A	XP_024308773.1:p.His425Asn
XM_024453006.1:c.1210C>A	XP_024308774.1:p.His404Asn
XR_001739705.1:n.3607-404G>T
XR_923313.2:n.4043-404G>T
NM_000312.4:c.1108C>A MANE Select	NP_000303.1:p.His370Asn
NM_001375602.1:c.1291C>A	NP_001362531.1:p.His431Asn
NM_001375603.1:c.1273C>A	NP_001362532.1:p.His425Asn
NM_001375604.1:c.1171C>A	NP_001362533.1:p.His391Asn
NM_001375605.1:c.1210C>A	NP_001362534.1:p.His404Asn
NM_001375606.1:c.1276C>A	NP_001362535.1:p.His426Asn
NM_001375607.1:c.1294C>A	NP_001362536.1:p.His432Asn
NM_001375608.1:c.1051C>A	NP_001362537.1:p.His351Asn
NM_001375609.1:c.1084C>A	NP_001362538.1:p.His362Asn
NM_001375610.1:c.1102C>A	NP_001362539.1:p.His368Asn
NM_001375611.1:c.1108C>A	NP_001362540.1:p.His370Asn
NM_001375613.1:c.1108C>A	NP_001362542.1:p.His370Asn