Canonical Allele Identifier: CA1619235119
Gene: PRRC2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622664T= , CM000668.2:g.31622664T= GRCh38
NC_000006.11:g.31590441T= , CM000668.1:g.31590441T= GRCh37
NC_000006.10:g.31698420T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-100-26T= MANE Select ENSP00000365201.2:n.-100-26T=
ENST00000376007.8:c.-63-63T= ENSP00000365175.4:n.-63-63T=
ENST00000376033.2:c.-100-26T= ENSP00000365201.2:n.-100-26T=
ENST00000469577.5:n.136-1597T=
NM_004638.3:c.-100-26T= NP_004629.3:n.-100-26T=
NM_080686.2:c.-63-63T= NP_542417.2:n.-63-63T=
XM_011514890.1:c.-63-63T= XP_011513192.1:n.-63-63T=
NM_004638.4:c.-100-26T= MANE Select NP_004629.3:n.-100-26T=
NM_080686.3:c.-63-63T= NP_542417.2:n.-63-63T=
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