Canonical Allele Identifier: CA1619240671
Gene: PRRC2A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31635335G= , CM000668.2:g.31635335G= GRCh38
NC_000006.11:g.31603112G= , CM000668.1:g.31603112G= GRCh37
NC_000006.10:g.31711091G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.5302-59G= MANE Select ENSP00000365201.2:n.5302-59G=
ENST00000376007.8:c.5302-59G= ENSP00000365175.4:n.5302-59G=
ENST00000376033.2:c.5302-59G= ENSP00000365201.2:n.5302-59G=
ENST00000469501.1:n.32-59G=
NM_004638.3:c.5302-59G= NP_004629.3:n.5302-59G=
NM_080686.2:c.5302-59G= NP_542417.2:n.5302-59G=
XM_011514890.1:c.5302-59G= XP_011513192.1:n.5302-59G=
XM_017011274.1:c.5302-59G= XP_016866763.1:n.5302-59G=
NM_004638.4:c.5302-59G= MANE Select NP_004629.3:n.5302-59G=
NM_080686.3:c.5302-59G= NP_542417.2:n.5302-59G=
Search 100 bp 5'
Search 100 bp 3'