Canonical Allele Identifier: CA2658450990
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29073074-G-GAAT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073074_29073075insAAT , CM000664.2:g.29073074_29073075insAAT GRCh38
NC_000002.11:g.29295940_29295941insAAT , CM000664.1:g.29295940_29295941insAAT GRCh37
NC_000002.10:g.29149444_29149445insAAT NCBI36
NG_021427.1:g.6187_6188insATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1187_1188insATT MANE Select ENSP00000332809.4:p.Thr396_Trp397insPhe
ENST00000331664.5:c.1187_1188insATT ENSP00000332809.4:p.Thr396_Trp397insPhe
NM_001029883.2:c.1187_1188insATT NP_001025054.1:p.Thr396_Trp397insPhe
XM_011532826.1:c.1187_1188insATT XP_011531128.1:p.Thr396_Trp397insPhe
XR_939901.1:n.185+3907_185+3908insAAT
XR_939902.1:n.173+3919_173+3920insAAT
NM_001029883.3:c.1187_1188insATT MANE Select NP_001025054.1:p.Thr396_Trp397insPhe
Search 100 bp 5'
Search 100 bp 3'