Canonical Allele Identifier: CA1241018017
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071215T= , CM000664.2:g.29071215T= GRCh38
NC_000002.11:g.29294081T= , CM000664.1:g.29294081T= GRCh37
NC_000002.10:g.29147585T= NCBI36
NG_021427.1:g.8047A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3047A= MANE Select ENSP00000332809.4:p.Tyr1016=
ENST00000331664.5:c.3047A= ENSP00000332809.4:p.Tyr1016=
NM_001029883.2:c.3047A= NP_001025054.1:p.Tyr1016=
XM_011532826.1:c.3047A= XP_011531128.1:p.Tyr1016=
XR_939901.1:n.185+2048T=
XR_939902.1:n.173+2060T=
NM_001029883.3:c.3047A= MANE Select NP_001025054.1:p.Tyr1016=