Canonical Allele Identifier: CA2194866052

Gene: ARPIN ARPIN-AP3S2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89904714A>T , CM000677.2:g.89904714A>T	GRCh38
NC_000015.9:g.90447946A>T , CM000677.1:g.90447946A>T	GRCh37
NC_000015.8:g.88248950A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357484.10:c.302-731T>A (ARPIN) MANE Select	ENSP00000350075.5:n.302-731T>A
ENST00000357484.9:c.302-731T>A (ARPIN)	ENSP00000350075.5:n.302-731T>A
ENST00000398333.7:c.302-731T>A (ARPIN-AP3S2)	ENSP00000381377.3:n.302-731T>A
ENST00000460685.1:c.14-731T>A (ARPIN)	ENSP00000453687.1:n.14-731T>A
ENST00000558648.5:c.14-731T>A (ARPIN-AP3S2)	ENSP00000453100.1:n.14-731T>A
ENST00000559629.1:c.14-1335T>A (ARPIN-AP3S2)	ENSP00000453637.1:n.14-1335T>A
NM_001199058.1:c.302-731T>A (ARPIN-AP3S2)	NP_001185987.1:n.302-731T>A
NM_001282380.1:c.14-731T>A (ARPIN)	NP_001269309.1:n.14-731T>A
NM_182616.3:c.302-731T>A (ARPIN)	NP_872422.1:n.302-731T>A
NM_182616.4:c.302-731T>A (ARPIN) MANE Select	NP_872422.1:n.302-731T>A
NM_001199058.2:c.302-731T>A (ARPIN-AP3S2)	NP_001185987.1:n.302-731T>A
NM_001282380.2:c.14-731T>A (ARPIN)	NP_001269309.1:n.14-731T>A