Canonical Allele Identifier: CA229328402

Gene: ZPR1

Linked Data

• dbSNP Id: rs997823922
• gnomAD v3: 11-116781525-T-TAA
• gnomAD v4: 11-116781525-T-TAA
• MyVariant Identifiers: chr11:g.116652241_116652242insAA (hg19) ; chr11:g.116781525_116781526insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116781530_116781531dup , CM000673.2:g.116781530_116781531dup	GRCh38
NC_000011.9:g.116652246_116652247dup , CM000673.1:g.116652246_116652247dup	GRCh37
NC_000011.8:g.116157456_116157457dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227322.8:c.1179+631_1179+632dup MANE Select	ENSP00000227322.3:n.1179+631_1179+632dup
ENST00000227322.7:c.1179+631_1179+632dup	ENSP00000227322.3:n.1179+631_1179+632dup
ENST00000429220.5:c.958+631_958+632dup
ENST00000444935.5:c.1091+1392_1091+1393dup
NM_003904.3:c.1179+631_1179+632dup	NP_003895.1:n.1179+631_1179+632dup
NM_001317086.1:c.1017+631_1017+632dup	NP_001304015.1:n.1017+631_1017+632dup
NM_003904.4:c.1179+631_1179+632dup	NP_003895.1:n.1179+631_1179+632dup
XR_001748023.2:n.2507+631_2507+632dup
NM_003904.5:c.1179+631_1179+632dup MANE Select	NP_003895.1:n.1179+631_1179+632dup
NM_001317086.2:c.1017+631_1017+632dup	NP_001304015.1:n.1017+631_1017+632dup