Canonical Allele Identifier: CA1241017350

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29070780_29070783delinsTCTG , CM000664.2:g.29070780_29070783delinsTCTG	GRCh38
NC_000002.11:g.29293646_29293649delinsTCTG , CM000664.1:g.29293646_29293649delinsTCTG	GRCh37
NC_000002.10:g.29147150_29147153delinsTCTG	NCBI36
NG_021427.1:g.8479_8482delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3479_3482delinsCAGA MANE Select	ENSP00000332809.4:p.Ala1160=
ENST00000331664.5:c.3479_3482delinsCAGA	ENSP00000332809.4:p.Ala1160=
NM_001029883.2:c.3479_3482delinsCAGA	NP_001025054.1:p.Ala1160=
XM_011532826.1:c.3479_3482delinsCAGA	XP_011531128.1:p.Ala1160=
XR_939901.1:n.185+1613_185+1616delinsTCTG
XR_939902.1:n.173+1625_173+1628delinsTCTG
NM_001029883.3:c.3479_3482delinsCAGA MANE Select	NP_001025054.1:p.Ala1160=