Canonical Allele Identifier: CA2578565746
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622751G>A , CM000668.2:g.31622751G>A GRCh38
NC_000006.11:g.31590528G>A , CM000668.1:g.31590528G>A GRCh37
NC_000006.10:g.31698507G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-39G>A MANE Select ENSP00000365201.2:n.-39G>A
ENST00000376007.8:c.-39G>A ENSP00000365175.4:n.-39G>A
ENST00000376033.2:c.-39G>A ENSP00000365201.2:n.-39G>A
ENST00000469577.5:n.136-1510G>A
NM_004638.3:c.-39G>A NP_004629.3:n.-39G>A
NM_080686.2:c.-39G>A NP_542417.2:n.-39G>A
XM_011514890.1:c.-39G>A XP_011513192.1:n.-39G>A
NM_004638.4:c.-39G>A MANE Select NP_004629.3:n.-39G>A
NM_080686.3:c.-39G>A NP_542417.2:n.-39G>A