Canonical Allele Identifier: CA2658448286
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs773072098
gnomAD v4: 2-29070723-G-GCTGCTCTCCGCTGCGAGT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070732_29070749dup , CM000664.2:g.29070732_29070749dup GRCh38
NC_000002.11:g.29293598_29293615dup , CM000664.1:g.29293598_29293615dup GRCh37
NC_000002.10:g.29147102_29147119dup NCBI36
NG_021427.1:g.8521_8538dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3521_3538dup MANE Select ENSP00000332809.4:p.Ala1179_Ala1180insAspSerGlnArgArgAla
ENST00000331664.5:c.3521_3538dup ENSP00000332809.4:p.Ala1179_Ala1180insAspSerGlnArgArgAla
NM_001029883.2:c.3521_3538dup NP_001025054.1:p.Ala1179_Ala1180insAspSerGlnArgArgAla
XM_011532826.1:c.3521_3538dup XP_011531128.1:p.Ala1179_Ala1180insAspSerGlnArgArgAla
XR_939901.1:n.185+1565_185+1582dup
XR_939902.1:n.173+1577_173+1594dup
NM_001029883.3:c.3521_3538dup MANE Select NP_001025054.1:p.Ala1179_Ala1180insAspSerGlnArgArgAla
Search 100 bp 5'
Search 100 bp 3'