Canonical Allele Identifier: CA1619240516

Gene: PRRC2A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635029_31635033delinsCCCTA , CM000668.2:g.31635029_31635033delinsCCCTA	GRCh38
NC_000006.11:g.31602806_31602810delinsCCCTA , CM000668.1:g.31602806_31602810delinsCCCTA	GRCh37
NC_000006.10:g.31710785_31710789delinsCCCTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5160+52_5160+56delinsCCCTA MANE Select	ENSP00000365201.2:n.5160+52_5160+56delinsCCCTA
ENST00000376007.8:c.5160+52_5160+56delinsCCCTA	ENSP00000365175.4:n.5160+52_5160+56delinsCCCTA
ENST00000376033.2:c.5160+52_5160+56delinsCCCTA	ENSP00000365201.2:n.5160+52_5160+56delinsCCCTA
ENST00000484787.1:n.571+52_571+56delinsCCCTA
NM_004638.3:c.5160+52_5160+56delinsCCCTA	NP_004629.3:n.5160+52_5160+56delinsCCCTA
NM_080686.2:c.5160+52_5160+56delinsCCCTA	NP_542417.2:n.5160+52_5160+56delinsCCCTA
XM_011514890.1:c.5160+52_5160+56delinsCCCTA	XP_011513192.1:n.5160+52_5160+56delinsCCCTA
XM_017011274.1:c.5160+52_5160+56delinsCCCTA	XP_016866763.1:n.5160+52_5160+56delinsCCCTA
NM_004638.4:c.5160+52_5160+56delinsCCCTA MANE Select	NP_004629.3:n.5160+52_5160+56delinsCCCTA
NM_080686.3:c.5160+52_5160+56delinsCCCTA	NP_542417.2:n.5160+52_5160+56delinsCCCTA