Canonical Allele Identifier: CA348401591

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183776G>C (hg19) ; chr2:g.127426200G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426200G>C , CM000664.2:g.127426200G>C	GRCh38
NC_000002.11:g.128183776G>C , CM000664.1:g.128183776G>C	GRCh37
NC_000002.10:g.127900246G>C	NCBI36
NG_016323.1:g.12781G>C , LRG_599:g.12781G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.651G>C MANE Select	ENSP00000234071.4:p.Met217Ile
ENST00000234071.7:c.651G>C	ENSP00000234071.3:p.Met217Ile
ENST00000402125.2:c.121-2157G>C
ENST00000409048.1:c.753G>C	ENSP00000386679.1:p.Met251Ile
ENST00000464089.1:n.237G>C
NM_000312.3:c.651G>C , LRG_599t1:c.651G>C	NP_000303.1:p.Met217Ile
XM_005263715.3:c.834G>C	XP_005263772.1:p.Met278Ile
XM_005263716.3:c.816G>C	XP_005263773.1:p.Met272Ile
XM_005263717.3:c.714G>C	XP_005263774.1:p.Met238Ile
XM_005263717.4:c.714G>C	XP_005263774.1:p.Met238Ile
XM_017004505.1:c.894G>C	XP_016859994.1:p.Met298Ile
XM_024453002.1:c.996G>C	XP_024308770.1:p.Met332Ile
XM_024453003.1:c.936G>C	XP_024308771.1:p.Met312Ile
XM_024453004.1:c.834G>C	XP_024308772.1:p.Met278Ile
XM_024453005.1:c.816G>C	XP_024308773.1:p.Met272Ile
XM_024453006.1:c.753G>C	XP_024308774.1:p.Met251Ile
XR_923313.2:n.4385C>G
NM_000312.4:c.651G>C MANE Select	NP_000303.1:p.Met217Ile
NM_001375602.1:c.834G>C	NP_001362531.1:p.Met278Ile
NM_001375603.1:c.816G>C	NP_001362532.1:p.Met272Ile
NM_001375604.1:c.714G>C	NP_001362533.1:p.Met238Ile
NM_001375605.1:c.753G>C	NP_001362534.1:p.Met251Ile
NM_001375606.1:c.819G>C	NP_001362535.1:p.Met273Ile
NM_001375607.1:c.837G>C	NP_001362536.1:p.Met279Ile
NM_001375608.1:c.594G>C	NP_001362537.1:p.Met198Ile
NM_001375609.1:c.627G>C	NP_001362538.1:p.Met209Ile
NM_001375610.1:c.645G>C	NP_001362539.1:p.Met215Ile
NM_001375611.1:c.651G>C	NP_001362540.1:p.Met217Ile
NM_001375613.1:c.651G>C	NP_001362542.1:p.Met217Ile