Canonical Allele Identifier: CA348401463

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183747G>T (hg19) ; chr2:g.127426171G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426171G>T , CM000664.2:g.127426171G>T	GRCh38
NC_000002.11:g.128183747G>T , CM000664.1:g.128183747G>T	GRCh37
NC_000002.10:g.127900217G>T	NCBI36
NG_016323.1:g.12752G>T , LRG_599:g.12752G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.622G>T MANE Select	ENSP00000234071.4:p.Val208Leu
ENST00000234071.7:c.622G>T	ENSP00000234071.3:p.Val208Leu
ENST00000402125.2:c.121-2186G>T
ENST00000409048.1:c.724G>T	ENSP00000386679.1:p.Val242Leu
ENST00000464089.1:n.208G>T
NM_000312.3:c.622G>T , LRG_599t1:c.622G>T	NP_000303.1:p.Val208Leu
XM_005263715.3:c.805G>T	XP_005263772.1:p.Val269Leu
XM_005263716.3:c.787G>T	XP_005263773.1:p.Val263Leu
XM_005263717.3:c.685G>T	XP_005263774.1:p.Val229Leu
XM_005263717.4:c.685G>T	XP_005263774.1:p.Val229Leu
XM_017004505.1:c.865G>T	XP_016859994.1:p.Val289Leu
XM_024453002.1:c.967G>T	XP_024308770.1:p.Val323Leu
XM_024453003.1:c.907G>T	XP_024308771.1:p.Val303Leu
XM_024453004.1:c.805G>T	XP_024308772.1:p.Val269Leu
XM_024453005.1:c.787G>T	XP_024308773.1:p.Val263Leu
XM_024453006.1:c.724G>T	XP_024308774.1:p.Val242Leu
XR_923313.2:n.4414C>A
NM_000312.4:c.622G>T MANE Select	NP_000303.1:p.Val208Leu
NM_001375602.1:c.805G>T	NP_001362531.1:p.Val269Leu
NM_001375603.1:c.787G>T	NP_001362532.1:p.Val263Leu
NM_001375604.1:c.685G>T	NP_001362533.1:p.Val229Leu
NM_001375605.1:c.724G>T	NP_001362534.1:p.Val242Leu
NM_001375606.1:c.790G>T	NP_001362535.1:p.Val264Leu
NM_001375607.1:c.808G>T	NP_001362536.1:p.Val270Leu
NM_001375608.1:c.565G>T	NP_001362537.1:p.Val189Leu
NM_001375609.1:c.598G>T	NP_001362538.1:p.Val200Leu
NM_001375610.1:c.616G>T	NP_001362539.1:p.Val206Leu
NM_001375611.1:c.622G>T	NP_001362540.1:p.Val208Leu
NM_001375613.1:c.622G>T	NP_001362542.1:p.Val208Leu