Canonical Allele Identifier: CA1241017915
Gene: PCARE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071046_29071048delinsGCT , CM000664.2:g.29071046_29071048delinsGCT GRCh38
NC_000002.11:g.29293912_29293914delinsGCT , CM000664.1:g.29293912_29293914delinsGCT GRCh37
NC_000002.10:g.29147416_29147418delinsGCT NCBI36
NG_021427.1:g.8214_8216delinsAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3214_3216delinsAGC MANE Select ENSP00000332809.4:p.Ser1072=
ENST00000331664.5:c.3214_3216delinsAGC ENSP00000332809.4:p.Ser1072=
NM_001029883.2:c.3214_3216delinsAGC NP_001025054.1:p.Ser1072=
XM_011532826.1:c.3214_3216delinsAGC XP_011531128.1:p.Ser1072=
XR_939901.1:n.185+1879_185+1881delinsGCT
XR_939902.1:n.173+1891_173+1893delinsGCT
NM_001029883.3:c.3214_3216delinsAGC MANE Select NP_001025054.1:p.Ser1072=