Canonical Allele Identifier: CA1619235559
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31623055T= , CM000668.2:g.31623055T= GRCh38
NC_000006.11:g.31590832T= , CM000668.1:g.31590832T= GRCh37
NC_000006.10:g.31698811T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.112+154T= MANE Select ENSP00000365201.2:n.112+154T=
ENST00000376007.8:c.112+154T= ENSP00000365175.4:n.112+154T=
ENST00000376033.2:c.112+154T= ENSP00000365201.2:n.112+154T=
ENST00000469577.5:n.136-1206T=
NM_004638.3:c.112+154T= NP_004629.3:n.112+154T=
NM_080686.2:c.112+154T= NP_542417.2:n.112+154T=
XM_011514890.1:c.112+154T= XP_011513192.1:n.112+154T=
XM_017011274.1:c.112+154T= XP_016866763.1:n.112+154T=
NM_004638.4:c.112+154T= MANE Select NP_004629.3:n.112+154T=
NM_080686.3:c.112+154T= NP_542417.2:n.112+154T=