Canonical Allele Identifier: CA55348435

Gene: PROC

Linked Data

• dbSNP Id: rs926009782
• gnomAD v2: 2-128183788-A-T
• gnomAD v4: 2-127426212-A-T
• MyVariant Identifiers: chr2:g.128183788A>T (hg19) ; chr2:g.127426212A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426212A>T , CM000664.2:g.127426212A>T	GRCh38
NC_000002.11:g.128183788A>T , CM000664.1:g.128183788A>T	GRCh37
NC_000002.10:g.127900258A>T	NCBI36
NG_016323.1:g.12793A>T , LRG_599:g.12793A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.663A>T MANE Select	ENSP00000234071.4:p.Gly221=
ENST00000234071.7:c.663A>T	ENSP00000234071.3:p.Gly221=
ENST00000402125.2:c.121-2145A>T
ENST00000409048.1:c.765A>T	ENSP00000386679.1:p.Gly255=
ENST00000464089.1:n.249A>T
NM_000312.3:c.663A>T , LRG_599t1:c.663A>T	NP_000303.1:p.Gly221=
XM_005263715.3:c.846A>T	XP_005263772.1:p.Gly282=
XM_005263716.3:c.828A>T	XP_005263773.1:p.Gly276=
XM_005263717.3:c.726A>T	XP_005263774.1:p.Gly242=
XM_005263717.4:c.726A>T	XP_005263774.1:p.Gly242=
XM_017004505.1:c.906A>T	XP_016859994.1:p.Gly302=
XM_024453002.1:c.1008A>T	XP_024308770.1:p.Gly336=
XM_024453003.1:c.948A>T	XP_024308771.1:p.Gly316=
XM_024453004.1:c.846A>T	XP_024308772.1:p.Gly282=
XM_024453005.1:c.828A>T	XP_024308773.1:p.Gly276=
XM_024453006.1:c.765A>T	XP_024308774.1:p.Gly255=
XR_923313.2:n.4373T>A
NM_000312.4:c.663A>T MANE Select	NP_000303.1:p.Gly221=
NM_001375602.1:c.846A>T	NP_001362531.1:p.Gly282=
NM_001375603.1:c.828A>T	NP_001362532.1:p.Gly276=
NM_001375604.1:c.726A>T	NP_001362533.1:p.Gly242=
NM_001375605.1:c.765A>T	NP_001362534.1:p.Gly255=
NM_001375606.1:c.831A>T	NP_001362535.1:p.Gly277=
NM_001375607.1:c.849A>T	NP_001362536.1:p.Gly283=
NM_001375608.1:c.606A>T	NP_001362537.1:p.Gly202=
NM_001375609.1:c.639A>T	NP_001362538.1:p.Gly213=
NM_001375610.1:c.657A>T	NP_001362539.1:p.Gly219=
NM_001375611.1:c.663A>T	NP_001362540.1:p.Gly221=
NM_001375613.1:c.663A>T	NP_001362542.1:p.Gly221=