Canonical Allele Identifier: CA1619241695
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31637435C= , CM000668.2:g.31637435C= GRCh38
NC_000006.11:g.31605212C= , CM000668.1:g.31605212C= GRCh37
NC_000006.10:g.31713191C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.6334-11C= MANE Select ENSP00000365201.2:n.6334-11C=
ENST00000376007.8:c.6334-11C= ENSP00000365175.4:n.6334-11C=
ENST00000376033.2:c.6334-11C= ENSP00000365201.2:n.6334-11C=
ENST00000462617.1:n.679C=
ENST00000482441.1:n.394-11C=
ENST00000492691.5:n.782C=
NM_004638.3:c.6334-11C= NP_004629.3:n.6334-11C=
NM_080686.2:c.6334-11C= NP_542417.2:n.6334-11C=
XM_011514890.1:c.6121-11C= XP_011513192.1:n.6121-11C=
XM_017011274.1:c.6121-11C= XP_016866763.1:n.6121-11C=
NM_004638.4:c.6334-11C= MANE Select NP_004629.3:n.6334-11C=
NM_080686.3:c.6334-11C= NP_542417.2:n.6334-11C=