Canonical Allele Identifier: CA348406362

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186368A>C (hg19) ; chr2:g.127428792A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428792A>C , CM000664.2:g.127428792A>C	GRCh38
NC_000002.11:g.128186368A>C , CM000664.1:g.128186368A>C	GRCh37
NC_000002.10:g.127902838A>C	NCBI36
NG_016323.1:g.15373A>C , LRG_599:g.15373A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1232A>C MANE Select	ENSP00000234071.4:p.His411Pro
ENST00000234071.7:c.1232A>C	ENSP00000234071.3:p.His411Pro
ENST00000402125.2:c.556A>C
ENST00000409048.1:c.1334A>C	ENSP00000386679.1:p.His445Pro
NM_000312.3:c.1232A>C , LRG_599t1:c.1232A>C	NP_000303.1:p.His411Pro
XM_005263715.3:c.1415A>C	XP_005263772.1:p.His472Pro
XM_005263716.3:c.1397A>C	XP_005263773.1:p.His466Pro
XM_005263717.3:c.1295A>C	XP_005263774.1:p.His432Pro
XR_923313.1:n.1332-528T>G
XM_005263717.4:c.1295A>C	XP_005263774.1:p.His432Pro
XM_017004505.1:c.1475A>C	XP_016859994.1:p.His492Pro
XM_024453002.1:c.1577A>C	XP_024308770.1:p.His526Pro
XM_024453003.1:c.1517A>C	XP_024308771.1:p.His506Pro
XM_024453004.1:c.1415A>C	XP_024308772.1:p.His472Pro
XM_024453005.1:c.1397A>C	XP_024308773.1:p.His466Pro
XM_024453006.1:c.1334A>C	XP_024308774.1:p.His445Pro
XR_001739705.1:n.3607-528T>G
XR_923313.2:n.4043-528T>G
NM_000312.4:c.1232A>C MANE Select	NP_000303.1:p.His411Pro
NM_001375602.1:c.1415A>C	NP_001362531.1:p.His472Pro
NM_001375603.1:c.1397A>C	NP_001362532.1:p.His466Pro
NM_001375604.1:c.1295A>C	NP_001362533.1:p.His432Pro
NM_001375605.1:c.1334A>C	NP_001362534.1:p.His445Pro
NM_001375606.1:c.1400A>C	NP_001362535.1:p.His467Pro
NM_001375607.1:c.1418A>C	NP_001362536.1:p.His473Pro
NM_001375608.1:c.1175A>C	NP_001362537.1:p.His392Pro
NM_001375609.1:c.1208A>C	NP_001362538.1:p.His403Pro
NM_001375610.1:c.1226A>C	NP_001362539.1:p.His409Pro
NM_001375611.1:c.1232A>C	NP_001362540.1:p.His411Pro
NM_001375613.1:c.1232A>C	NP_001362542.1:p.His411Pro