Canonical Allele Identifier: CA2578565717
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622695_31622700del , CM000668.2:g.31622695_31622700del GRCh38
NC_000006.11:g.31590472_31590477del , CM000668.1:g.31590472_31590477del GRCh37
NC_000006.10:g.31698451_31698456del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-95_-90del MANE Select ENSP00000365201.2:n.-95_-90del
ENST00000376007.8:c.-63-32_-63-27del ENSP00000365175.4:n.-63-32_-63-27del
ENST00000376033.2:c.-95_-90del ENSP00000365201.2:n.-95_-90del
ENST00000469577.5:n.136-1566_136-1561del
NM_004638.3:c.-95_-90del NP_004629.3:n.-95_-90del
NM_080686.2:c.-63-32_-63-27del NP_542417.2:n.-63-32_-63-27del
XM_011514890.1:c.-63-32_-63-27del XP_011513192.1:n.-63-32_-63-27del
NM_004638.4:c.-95_-90del MANE Select NP_004629.3:n.-95_-90del
NM_080686.3:c.-63-32_-63-27del NP_542417.2:n.-63-32_-63-27del