Canonical Allele Identifier: CA2002735688

Gene: ZPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116781442_116781445delinsACTT , CM000673.2:g.116781442_116781445delinsACTT	GRCh38
NC_000011.9:g.116652158_116652161delinsACTT , CM000673.1:g.116652158_116652161delinsACTT	GRCh37
NC_000011.8:g.116157368_116157371delinsACTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227322.8:c.1179+713_1179+716delinsAAGT MANE Select	ENSP00000227322.3:n.1179+713_1179+716delinsAAGT
ENST00000227322.7:c.1179+713_1179+716delinsAAGT	ENSP00000227322.3:n.1179+713_1179+716delinsAAGT
ENST00000429220.5:c.958+713_958+716delinsAAGT
ENST00000444935.5:c.1091+1474_1091+1477delinsAAGT
NM_003904.3:c.1179+713_1179+716delinsAAGT	NP_003895.1:n.1179+713_1179+716delinsAAGT
NM_001317086.1:c.1017+713_1017+716delinsAAGT	NP_001304015.1:n.1017+713_1017+716delinsAAGT
NM_003904.4:c.1179+713_1179+716delinsAAGT	NP_003895.1:n.1179+713_1179+716delinsAAGT
XR_001748023.2:n.2507+713_2507+716delinsAAGT
NM_003904.5:c.1179+713_1179+716delinsAAGT MANE Select	NP_003895.1:n.1179+713_1179+716delinsAAGT
NM_001317086.2:c.1017+713_1017+716delinsAAGT	NP_001304015.1:n.1017+713_1017+716delinsAAGT