Canonical Allele Identifier: CA2658449982
Gene: PCARE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071136_29071162dup , CM000664.2:g.29071136_29071162dup GRCh38
NC_000002.11:g.29294002_29294028dup , CM000664.1:g.29294002_29294028dup GRCh37
NC_000002.10:g.29147506_29147532dup NCBI36
NG_021427.1:g.8100_8126dup

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3100_3126dup MANE Select ENSP00000332809.4:p.Pro1042_Thr1043insVal...
ENST00000331664.5:c.3100_3126dup ENSP00000332809.4:p.Pro1042_Thr1043insVal...
NM_001029883.2:c.3100_3126dup NP_001025054.1:p.Pro1042_Thr1043insValSer...
XM_011532826.1:c.3100_3126dup XP_011531128.1:p.Pro1042_Thr1043insValSer...
XR_939901.1:n.185+1969_185+1995dup
XR_939902.1:n.173+1981_173+2007dup
NM_001029883.3:c.3100_3126dup MANE Select NP_001025054.1:p.Pro1042_Thr1043insValSer...