Canonical Allele Identifier: CA1619240422
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs1777124159
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31634869dup , CM000668.2:g.31634869dup GRCh38
NC_000006.11:g.31602646dup , CM000668.1:g.31602646dup GRCh37
NC_000006.10:g.31710625dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5052dup MANE Select ENSP00000365201.2:p.Lys1685GlnfsTer15
ENST00000376007.8:c.5052dup ENSP00000365175.4:p.Lys1685GlnfsTer15
ENST00000376033.2:c.5052dup ENSP00000365201.2:p.Lys1685GlnfsTer15
ENST00000484787.1:n.463dup
NM_004638.3:c.5052dup NP_004629.3:p.Lys1685GlnfsTer15
NM_080686.2:c.5052dup NP_542417.2:p.Lys1685GlnfsTer15
XM_011514890.1:c.5052dup XP_011513192.1:p.Lys1685GlnfsTer15
XM_017011274.1:c.5052dup XP_016866763.1:p.Lys1685GlnfsTer15
NM_004638.4:c.5052dup MANE Select NP_004629.3:p.Lys1685GlnfsTer15
NM_080686.3:c.5052dup NP_542417.2:p.Lys1685GlnfsTer15
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Search 100 bp 3'