Canonical Allele Identifier: CA566690426
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v2: 6-31602887-CT-C
MyVariant Identifiers: chr6:g.31602888del (hg19) chr6:g.31635111del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635113del , CM000668.2:g.31635113del GRCh38
NC_000006.11:g.31602890del , CM000668.1:g.31602890del GRCh37
NC_000006.10:g.31710869del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5161-19del MANE Select ENSP00000365201.2:n.5161-19del
ENST00000376007.8:c.5161-19del ENSP00000365175.4:n.5161-19del
ENST00000376033.2:c.5161-19del ENSP00000365201.2:n.5161-19del
ENST00000484787.1:n.572-19del
NM_004638.3:c.5161-19del NP_004629.3:n.5161-19del
NM_080686.2:c.5161-19del NP_542417.2:n.5161-19del
XM_011514890.1:c.5161-19del XP_011513192.1:n.5161-19del
XM_017011274.1:c.5161-19del XP_016866763.1:n.5161-19del
NM_004638.4:c.5161-19del MANE Select NP_004629.3:n.5161-19del
NM_080686.3:c.5161-19del NP_542417.2:n.5161-19del
Search 100 bp 5'
Search 100 bp 3'