Canonical Allele Identifier: CA2749314516
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071037_29071038insAGA , CM000664.2:g.29071037_29071038insAGA GRCh38
NC_000002.11:g.29293903_29293904insAGA , CM000664.1:g.29293903_29293904insAGA GRCh37
NC_000002.10:g.29147407_29147408insAGA NCBI36
NG_021427.1:g.8224_8225insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3224_3225insTCT MANE Select ENSP00000332809.4:p.Thr1075_Gln1076insLeu
ENST00000331664.5:c.3224_3225insTCT ENSP00000332809.4:p.Thr1075_Gln1076insLeu
NM_001029883.2:c.3224_3225insTCT NP_001025054.1:p.Thr1075_Gln1076insLeu
XM_011532826.1:c.3224_3225insTCT XP_011531128.1:p.Thr1075_Gln1076insLeu
XR_939901.1:n.185+1870_185+1871insAGA
XR_939902.1:n.173+1882_173+1883insAGA
NM_001029883.3:c.3224_3225insTCT MANE Select NP_001025054.1:p.Thr1075_Gln1076insLeu
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Search 100 bp 3'