Canonical Allele Identifier: CA1619240489

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1777148949
• gnomAD v4: 6-31634994-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31634994G>C , CM000668.2:g.31634994G>C	GRCh38
NC_000006.11:g.31602771G>C , CM000668.1:g.31602771G>C	GRCh37
NC_000006.10:g.31710750G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5160+17G>C MANE Select	ENSP00000365201.2:n.5160+17G>C
ENST00000376007.8:c.5160+17G>C	ENSP00000365175.4:n.5160+17G>C
ENST00000376033.2:c.5160+17G>C	ENSP00000365201.2:n.5160+17G>C
ENST00000484787.1:n.571+17G>C
NM_004638.3:c.5160+17G>C	NP_004629.3:n.5160+17G>C
NM_080686.2:c.5160+17G>C	NP_542417.2:n.5160+17G>C
XM_011514890.1:c.5160+17G>C	XP_011513192.1:n.5160+17G>C
XM_017011274.1:c.5160+17G>C	XP_016866763.1:n.5160+17G>C
NM_004638.4:c.5160+17G>C MANE Select	NP_004629.3:n.5160+17G>C
NM_080686.3:c.5160+17G>C	NP_542417.2:n.5160+17G>C