Canonical Allele Identifier: CA2578565719
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622692G>T , CM000668.2:g.31622692G>T GRCh38
NC_000006.11:g.31590469G>T , CM000668.1:g.31590469G>T GRCh37
NC_000006.10:g.31698448G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-98G>T MANE Select ENSP00000365201.2:n.-98G>T
ENST00000376007.8:c.-63-35G>T ENSP00000365175.4:n.-63-35G>T
ENST00000376033.2:c.-98G>T ENSP00000365201.2:n.-98G>T
ENST00000469577.5:n.136-1569G>T
NM_004638.3:c.-98G>T NP_004629.3:n.-98G>T
NM_080686.2:c.-63-35G>T NP_542417.2:n.-63-35G>T
XM_011514890.1:c.-63-35G>T XP_011513192.1:n.-63-35G>T
NM_004638.4:c.-98G>T MANE Select NP_004629.3:n.-98G>T
NM_080686.3:c.-63-35G>T NP_542417.2:n.-63-35G>T