Canonical Allele Identifier: CA348401543

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183768G>T (hg19) ; chr2:g.127426192G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426192G>T , CM000664.2:g.127426192G>T	GRCh38
NC_000002.11:g.128183768G>T , CM000664.1:g.128183768G>T	GRCh37
NC_000002.10:g.127900238G>T	NCBI36
NG_016323.1:g.12773G>T , LRG_599:g.12773G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.643G>T MANE Select	ENSP00000234071.4:p.Gly215Trp
ENST00000234071.7:c.643G>T	ENSP00000234071.3:p.Gly215Trp
ENST00000402125.2:c.121-2165G>T
ENST00000409048.1:c.745G>T	ENSP00000386679.1:p.Gly249Trp
ENST00000464089.1:n.229G>T
NM_000312.3:c.643G>T , LRG_599t1:c.643G>T	NP_000303.1:p.Gly215Trp
XM_005263715.3:c.826G>T	XP_005263772.1:p.Gly276Trp
XM_005263716.3:c.808G>T	XP_005263773.1:p.Gly270Trp
XM_005263717.3:c.706G>T	XP_005263774.1:p.Gly236Trp
XM_005263717.4:c.706G>T	XP_005263774.1:p.Gly236Trp
XM_017004505.1:c.886G>T	XP_016859994.1:p.Gly296Trp
XM_024453002.1:c.988G>T	XP_024308770.1:p.Gly330Trp
XM_024453003.1:c.928G>T	XP_024308771.1:p.Gly310Trp
XM_024453004.1:c.826G>T	XP_024308772.1:p.Gly276Trp
XM_024453005.1:c.808G>T	XP_024308773.1:p.Gly270Trp
XM_024453006.1:c.745G>T	XP_024308774.1:p.Gly249Trp
XR_923313.2:n.4393C>A
NM_000312.4:c.643G>T MANE Select	NP_000303.1:p.Gly215Trp
NM_001375602.1:c.826G>T	NP_001362531.1:p.Gly276Trp
NM_001375603.1:c.808G>T	NP_001362532.1:p.Gly270Trp
NM_001375604.1:c.706G>T	NP_001362533.1:p.Gly236Trp
NM_001375605.1:c.745G>T	NP_001362534.1:p.Gly249Trp
NM_001375606.1:c.811G>T	NP_001362535.1:p.Gly271Trp
NM_001375607.1:c.829G>T	NP_001362536.1:p.Gly277Trp
NM_001375608.1:c.586G>T	NP_001362537.1:p.Gly196Trp
NM_001375609.1:c.619G>T	NP_001362538.1:p.Gly207Trp
NM_001375610.1:c.637G>T	NP_001362539.1:p.Gly213Trp
NM_001375611.1:c.643G>T	NP_001362540.1:p.Gly215Trp
NM_001375613.1:c.643G>T	NP_001362542.1:p.Gly215Trp