Canonical Allele Identifier: CA363364947
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635271A>C , CM000668.2:g.31635271A>C GRCh38
NC_000006.11:g.31603048A>C , CM000668.1:g.31603048A>C GRCh37
NC_000006.10:g.31711027A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.5300A>C MANE Select ENSP00000365201.2:p.Lys1767Thr
ENST00000376007.8:c.5300A>C ENSP00000365175.4:p.Lys1767Thr
ENST00000376033.2:c.5300A>C ENSP00000365201.2:p.Lys1767Thr
ENST00000469501.1:n.30A>C
ENST00000484787.1:n.711A>C
NM_004638.3:c.5300A>C NP_004629.3:p.Lys1767Thr
NM_080686.2:c.5300A>C NP_542417.2:p.Lys1767Thr
XM_011514890.1:c.5300A>C XP_011513192.1:p.Lys1767Thr
XM_017011274.1:c.5300A>C XP_016866763.1:p.Lys1767Thr
NM_004638.4:c.5300A>C MANE Select NP_004629.3:p.Lys1767Thr
NM_080686.3:c.5300A>C NP_542417.2:p.Lys1767Thr