Canonical Allele Identifier: CA1087468128

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1777156942
• gnomAD v3: 6-31635029-CCCTA-C
• gnomAD v4: 6-31635029-CCCTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635033_31635036del , CM000668.2:g.31635033_31635036del	GRCh38
NC_000006.11:g.31602810_31602813del , CM000668.1:g.31602810_31602813del	GRCh37
NC_000006.10:g.31710789_31710792del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5160+56_5160+59del MANE Select	ENSP00000365201.2:n.5160+56_5160+59del
ENST00000376007.8:c.5160+56_5160+59del	ENSP00000365175.4:n.5160+56_5160+59del
ENST00000376033.2:c.5160+56_5160+59del	ENSP00000365201.2:n.5160+56_5160+59del
ENST00000484787.1:n.571+56_571+59del
NM_004638.3:c.5160+56_5160+59del	NP_004629.3:n.5160+56_5160+59del
NM_080686.2:c.5160+56_5160+59del	NP_542417.2:n.5160+56_5160+59del
XM_011514890.1:c.5160+56_5160+59del	XP_011513192.1:n.5160+56_5160+59del
XM_017011274.1:c.5160+56_5160+59del	XP_016866763.1:n.5160+56_5160+59del
NM_004638.4:c.5160+56_5160+59del MANE Select	NP_004629.3:n.5160+56_5160+59del
NM_080686.3:c.5160+56_5160+59del	NP_542417.2:n.5160+56_5160+59del