Canonical Allele Identifier: CA2677997596

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31635351-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635351_31635352insA , CM000668.2:g.31635351_31635352insA	GRCh38
NC_000006.11:g.31603128_31603129insA , CM000668.1:g.31603128_31603129insA	GRCh37
NC_000006.10:g.31711107_31711108insA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376033.3:c.5302-43_5302-42insA MANE Select	ENSP00000365201.2:n.5302-43_5302-42insA
ENST00000376007.8:c.5302-43_5302-42insA	ENSP00000365175.4:n.5302-43_5302-42insA
ENST00000376033.2:c.5302-43_5302-42insA	ENSP00000365201.2:n.5302-43_5302-42insA
ENST00000469501.1:n.32-43_32-42insA
NM_004638.3:c.5302-43_5302-42insA	NP_004629.3:n.5302-43_5302-42insA
NM_080686.2:c.5302-43_5302-42insA	NP_542417.2:n.5302-43_5302-42insA
XM_011514890.1:c.5302-43_5302-42insA	XP_011513192.1:n.5302-43_5302-42insA
XM_017011274.1:c.5302-43_5302-42insA	XP_016866763.1:n.5302-43_5302-42insA
NM_004638.4:c.5302-43_5302-42insA MANE Select	NP_004629.3:n.5302-43_5302-42insA
NM_080686.3:c.5302-43_5302-42insA	NP_542417.2:n.5302-43_5302-42insA