Canonical Allele Identifier: CA1241018952
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29072953_29072956delinsTGGA , CM000664.2:g.29072953_29072956delinsTGGA GRCh38
NC_000002.11:g.29295819_29295822delinsTGGA , CM000664.1:g.29295819_29295822delinsTGGA GRCh37
NC_000002.10:g.29149323_29149326delinsTGGA NCBI36
NG_021427.1:g.6306_6309delinsTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1306_1309delinsTCCA MANE Select ENSP00000332809.4:p.Ser436=
ENST00000331664.5:c.1306_1309delinsTCCA ENSP00000332809.4:p.Ser436=
NM_001029883.2:c.1306_1309delinsTCCA NP_001025054.1:p.Ser436=
XM_011532826.1:c.1306_1309delinsTCCA XP_011531128.1:p.Ser436=
XR_939901.1:n.185+3786_185+3789delinsTGGA
XR_939902.1:n.173+3798_173+3801delinsTGGA
NM_001029883.3:c.1306_1309delinsTCCA MANE Select NP_001025054.1:p.Ser436=