Canonical Allele Identifier: CA2749314514
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071030_29071031insACA , CM000664.2:g.29071030_29071031insACA GRCh38
NC_000002.11:g.29293896_29293897insACA , CM000664.1:g.29293896_29293897insACA GRCh37
NC_000002.10:g.29147400_29147401insACA NCBI36
NG_021427.1:g.8231_8232insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3231_3232insTGT MANE Select ENSP00000332809.4:p.His1077_Pro1078insCys
ENST00000331664.5:c.3231_3232insTGT ENSP00000332809.4:p.His1077_Pro1078insCys
NM_001029883.2:c.3231_3232insTGT NP_001025054.1:p.His1077_Pro1078insCys
XM_011532826.1:c.3231_3232insTGT XP_011531128.1:p.His1077_Pro1078insCys
XR_939901.1:n.185+1863_185+1864insACA
XR_939902.1:n.173+1875_173+1876insACA
NM_001029883.3:c.3231_3232insTGT MANE Select NP_001025054.1:p.His1077_Pro1078insCys
Search 100 bp 5'
Search 100 bp 3'