Canonical Allele Identifier: CA1619235256

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1775438561

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622768_31622769dup , CM000668.2:g.31622768_31622769dup	GRCh38
NC_000006.11:g.31590545_31590546dup , CM000668.1:g.31590545_31590546dup	GRCh37
NC_000006.10:g.31698524_31698525dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-22_-21dup MANE Select	ENSP00000365201.2:n.-22_-21dup
ENST00000376007.8:c.-22_-21dup	ENSP00000365175.4:n.-22_-21dup
ENST00000376033.2:c.-22_-21dup	ENSP00000365201.2:n.-22_-21dup
ENST00000469577.5:n.136-1493_136-1492dup
NM_004638.3:c.-22_-21dup	NP_004629.3:n.-22_-21dup
NM_080686.2:c.-22_-21dup	NP_542417.2:n.-22_-21dup
XM_011514890.1:c.-22_-21dup	XP_011513192.1:n.-22_-21dup
NM_004638.4:c.-22_-21dup MANE Select	NP_004629.3:n.-22_-21dup
NM_080686.3:c.-22_-21dup	NP_542417.2:n.-22_-21dup