Canonical Allele Identifier: CA2437590177

Gene: NEXMIF

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74740939_74740942delinsCTTG , CM000685.2:g.74740939_74740942delinsCTTG	GRCh38
NC_000023.10:g.73960774_73960777delinsCTTG , CM000685.1:g.73960774_73960777delinsCTTG	GRCh37
NC_000023.9:g.73877499_73877502delinsCTTG	NCBI36
NG_027726.1:g.189511_189514delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000055682.12:c.3615_3618delinsCAAG MANE Select	ENSP00000055682.5:p.Asn1205=
ENST00000616200.2:c.3615_3618delinsCAAG	ENSP00000480284.1:p.Asn1205=
ENST00000642681.2:c.3615_3618delinsCAAG	ENSP00000495800.1:p.Asn1205=
ENST00000055682.10:c.3615_3618delinsCAAG	ENSP00000055682.5:p.Asn1205=
ENST00000616200.1:c.3615_3618delinsCAAG	ENSP00000480284.1:p.Asn1205=
NM_001008537.2:c.3615_3618delinsCAAG	NP_001008537.1:p.Asn1205=
XM_011530935.1:c.3615_3618delinsCAAG	XP_011529237.1:p.Asn1205=
NM_001008537.3:c.3615_3618delinsCAAG MANE Select	NP_001008537.1:p.Asn1205=