Canonical Allele Identifier: CA2490796188

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218815_15218821delinsAAAGAAC , CM000664.2:g.15218815_15218821delinsAAAGAAC	GRCh38
NC_000002.11:g.15358939_15358945delinsAAAGAAC , CM000664.1:g.15358939_15358945delinsAAAGAAC	GRCh37
NC_000002.10:g.15276390_15276396delinsAAAGAAC	NCBI36
NG_032964.1:g.347528_347534delinsGTTCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4370_4376delinsGTTCTTT
ENST00000700062.1:c.4426+13601_4426+13607delinsGTTCTTT
ENST00000700063.1:c.895_901delinsGTTCTTT
ENST00000700064.1:c.2240_2246delinsGTTCTTT
ENST00000281513.10:c.6384_6390delinsGTTCTTT MANE Select	ENSP00000281513.5:p.Val2128=
ENST00000281513.9:c.6384_6390delinsGTTCTTT	ENSP00000281513.5:p.Val2128=
ENST00000417461.5:c.512+13601_512+13607delinsGTTCTTT	ENSP00000392421.1:n.512+13601_512+13607delinsGTTCTTT
ENST00000442506.5:c.3527_3533delinsGTTCTTT
NM_015909.3:c.6384_6390delinsGTTCTTT	NP_056993.2:p.Val2128=
NR_052013.2:n.6280+13601_6280+13607delinsGTTCTTT
XM_011510357.1:c.6255_6261delinsGTTCTTT	XP_011508659.1:p.Val2085=
XM_011510358.1:c.6384_6390delinsGTTCTTT	XP_011508660.1:p.Val2128=
XM_011510359.1:c.5745_5751delinsGTTCTTT	XP_011508661.1:p.Val1915=
XM_011510360.1:c.4185_4191delinsGTTCTTT	XP_011508662.1:p.Val1395=
XM_011510361.1:c.4176_4182delinsGTTCTTT	XP_011508663.1:p.Val1392=
XM_011510357.2:c.6255_6261delinsGTTCTTT	XP_011508659.1:p.Val2085=
XM_011510358.2:c.6384_6390delinsGTTCTTT	XP_011508660.1:p.Val2128=
XM_011510360.2:c.4185_4191delinsGTTCTTT	XP_011508662.1:p.Val1395=
XM_011510361.2:c.4176_4182delinsGTTCTTT	XP_011508663.1:p.Val1392=
XM_017004317.1:c.6384_6390delinsGTTCTTT	XP_016859806.1:p.Val2128=
XM_024452961.1:c.5745_5751delinsGTTCTTT	XP_024308729.1:p.Val1915=
NM_015909.4:c.6384_6390delinsGTTCTTT MANE Select	NP_056993.2:p.Val2128=
NR_052013.3:n.6266+13601_6266+13607delinsGTTCTTT