Canonical Allele Identifier: CA348406302

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186354G>C (hg19) ; chr2:g.127428778G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428778G>C , CM000664.2:g.127428778G>C	GRCh38
NC_000002.11:g.128186354G>C , CM000664.1:g.128186354G>C	GRCh37
NC_000002.10:g.127902824G>C	NCBI36
NG_016323.1:g.15359G>C , LRG_599:g.15359G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1218G>C MANE Select	ENSP00000234071.4:p.Met406Ile
ENST00000234071.7:c.1218G>C	ENSP00000234071.3:p.Met406Ile
ENST00000402125.2:c.542G>C
ENST00000409048.1:c.1320G>C	ENSP00000386679.1:p.Met440Ile
NM_000312.3:c.1218G>C , LRG_599t1:c.1218G>C	NP_000303.1:p.Met406Ile
XM_005263715.3:c.1401G>C	XP_005263772.1:p.Met467Ile
XM_005263716.3:c.1383G>C	XP_005263773.1:p.Met461Ile
XM_005263717.3:c.1281G>C	XP_005263774.1:p.Met427Ile
XR_923313.1:n.1332-514C>G
XM_005263717.4:c.1281G>C	XP_005263774.1:p.Met427Ile
XM_017004505.1:c.1461G>C	XP_016859994.1:p.Met487Ile
XM_024453002.1:c.1563G>C	XP_024308770.1:p.Met521Ile
XM_024453003.1:c.1503G>C	XP_024308771.1:p.Met501Ile
XM_024453004.1:c.1401G>C	XP_024308772.1:p.Met467Ile
XM_024453005.1:c.1383G>C	XP_024308773.1:p.Met461Ile
XM_024453006.1:c.1320G>C	XP_024308774.1:p.Met440Ile
XR_001739705.1:n.3607-514C>G
XR_923313.2:n.4043-514C>G
NM_000312.4:c.1218G>C MANE Select	NP_000303.1:p.Met406Ile
NM_001375602.1:c.1401G>C	NP_001362531.1:p.Met467Ile
NM_001375603.1:c.1383G>C	NP_001362532.1:p.Met461Ile
NM_001375604.1:c.1281G>C	NP_001362533.1:p.Met427Ile
NM_001375605.1:c.1320G>C	NP_001362534.1:p.Met440Ile
NM_001375606.1:c.1386G>C	NP_001362535.1:p.Met462Ile
NM_001375607.1:c.1404G>C	NP_001362536.1:p.Met468Ile
NM_001375608.1:c.1161G>C	NP_001362537.1:p.Met387Ile
NM_001375609.1:c.1194G>C	NP_001362538.1:p.Met398Ile
NM_001375610.1:c.1212G>C	NP_001362539.1:p.Met404Ile
NM_001375611.1:c.1218G>C	NP_001362540.1:p.Met406Ile
NM_001375613.1:c.1218G>C	NP_001362542.1:p.Met406Ile