Canonical Allele Identifier: CA1241013482

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073159_29073168delinsTGCTTGCCCA , CM000664.2:g.29073159_29073168delinsTGCTTGCCCA	GRCh38
NC_000002.11:g.29296025_29296034delinsTGCTTGCCCA , CM000664.1:g.29296025_29296034delinsTGCTTGCCCA	GRCh37
NC_000002.10:g.29149529_29149538delinsTGCTTGCCCA	NCBI36
NG_021427.1:g.6094_6103delinsTGGGCAAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1094_1103delinsTGGGCAAGCA MANE Select	ENSP00000332809.4:p.Leu365=
ENST00000331664.5:c.1094_1103delinsTGGGCAAGCA	ENSP00000332809.4:p.Leu365=
NM_001029883.2:c.1094_1103delinsTGGGCAAGCA	NP_001025054.1:p.Leu365=
XM_011532826.1:c.1094_1103delinsTGGGCAAGCA	XP_011531128.1:p.Leu365=
XR_939901.1:n.185+3992_185+4001delinsTGCTTGCCCA
XR_939902.1:n.173+4004_173+4013delinsTGCTTGCCCA
NM_001029883.3:c.1094_1103delinsTGGGCAAGCA MANE Select	NP_001025054.1:p.Leu365=