Canonical Allele Identifier: CA1619240509

Gene: PRRC2A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635018_31635033delinsTCTGACTTTGGCCCTA , CM000668.2:g.31635018_31635033delinsTCTGACTTTGGCCCTA	GRCh38
NC_000006.11:g.31602795_31602810delinsTCTGACTTTGGCCCTA , CM000668.1:g.31602795_31602810delinsTCTGACTTTGGCCCTA	GRCh37
NC_000006.10:g.31710774_31710789delinsTCTGACTTTGGCCCTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA MANE Select	ENSP00000365201.2:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA
ENST00000376007.8:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA	ENSP00000365175.4:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA
ENST00000376033.2:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA	ENSP00000365201.2:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA
ENST00000484787.1:n.571+41_571+56delinsTCTGACTTTGGCCCTA
NM_004638.3:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA	NP_004629.3:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA
NM_080686.2:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA	NP_542417.2:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA
XM_011514890.1:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA	XP_011513192.1:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA
XM_017011274.1:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA	XP_016866763.1:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA
NM_004638.4:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA MANE Select	NP_004629.3:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA
NM_080686.3:c.5160+41_5160+56delinsTCTGACTTTGGCCCTA	NP_542417.2:n.5160+41_5160+56delinsTCTGACTTTGGCCCTA