Canonical Allele Identifier: CA2576924622

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29071232_29071233insA , CM000664.2:g.29071232_29071233insA	GRCh38
NC_000002.11:g.29294098_29294099insA , CM000664.1:g.29294098_29294099insA	GRCh37
NC_000002.10:g.29147602_29147603insA	NCBI36
NG_021427.1:g.8029_8030insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3029_3030insT MANE Select	ENSP00000332809.4:p.Ser1011GlufsTer?
ENST00000331664.5:c.3029_3030insT	ENSP00000332809.4:p.Ser1011GlufsTer?
NM_001029883.2:c.3029_3030insT	NP_001025054.1:p.Ser1011GlufsTer?
XM_011532826.1:c.3029_3030insT	XP_011531128.1:p.Ser1011GlufsTer?
XR_939901.1:n.185+2065_185+2066insA
XR_939902.1:n.173+2077_173+2078insA
NM_001029883.3:c.3029_3030insT MANE Select	NP_001025054.1:p.Ser1011GlufsTer?