Canonical Allele Identifier: CA1619241694
Gene: PRRC2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31637434C= , CM000668.2:g.31637434C= GRCh38
NC_000006.11:g.31605211C= , CM000668.1:g.31605211C= GRCh37
NC_000006.10:g.31713190C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.6334-12C= MANE Select ENSP00000365201.2:n.6334-12C=
ENST00000376007.8:c.6334-12C= ENSP00000365175.4:n.6334-12C=
ENST00000376033.2:c.6334-12C= ENSP00000365201.2:n.6334-12C=
ENST00000462617.1:n.678C=
ENST00000482441.1:n.394-12C=
ENST00000492691.5:n.781C=
NM_004638.3:c.6334-12C= NP_004629.3:n.6334-12C=
NM_080686.2:c.6334-12C= NP_542417.2:n.6334-12C=
XM_011514890.1:c.6121-12C= XP_011513192.1:n.6121-12C=
XM_017011274.1:c.6121-12C= XP_016866763.1:n.6121-12C=
NM_004638.4:c.6334-12C= MANE Select NP_004629.3:n.6334-12C=
NM_080686.3:c.6334-12C= NP_542417.2:n.6334-12C=
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