Canonical Allele Identifier: CA1241018062
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071294_29071295delinsCA , CM000664.2:g.29071294_29071295delinsCA GRCh38
NC_000002.11:g.29294160_29294161delinsCA , CM000664.1:g.29294160_29294161delinsCA GRCh37
NC_000002.10:g.29147664_29147665delinsCA NCBI36
NG_021427.1:g.7967_7968delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.2967_2968delinsTG MANE Select ENSP00000332809.4:p.Pro989=
ENST00000331664.5:c.2967_2968delinsTG ENSP00000332809.4:p.Pro989=
NM_001029883.2:c.2967_2968delinsTG NP_001025054.1:p.Pro989=
XM_011532826.1:c.2967_2968delinsTG XP_011531128.1:p.Pro989=
XR_939901.1:n.185+2127_185+2128delinsCA
XR_939902.1:n.173+2139_173+2140delinsCA
NM_001029883.3:c.2967_2968delinsTG MANE Select NP_001025054.1:p.Pro989=
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Search 100 bp 3'