Canonical Allele Identifier: CA2490879614

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402242_15402244delinsGAT , CM000664.2:g.15402242_15402244delinsGAT	GRCh38
NC_000002.11:g.15542366_15542368delinsGAT , CM000664.1:g.15542366_15542368delinsGAT	GRCh37
NC_000002.10:g.15459817_15459819delinsGAT	NCBI36
NG_032964.1:g.164105_164107delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1092_1094delinsATC
ENST00000700062.1:c.1092_1094delinsATC
ENST00000700065.1:n.3008_3010delinsATC
ENST00000281513.10:c.2995_2997delinsATC MANE Select	ENSP00000281513.5:p.Ile999=
ENST00000281513.9:c.2995_2997delinsATC	ENSP00000281513.5:p.Ile999=
ENST00000429842.1:c.287_289delinsATC
ENST00000441755.5:c.136_138delinsATC	ENSP00000396501.1:p.Ile46=
ENST00000442506.5:c.138_140delinsATC
NM_015909.3:c.2995_2997delinsATC	NP_056993.2:p.Ile999=
NR_052013.2:n.3039_3041delinsATC
XM_011510357.1:c.2866_2868delinsATC	XP_011508659.1:p.Ile956=
XM_011510358.1:c.2995_2997delinsATC	XP_011508660.1:p.Ile999=
XM_011510359.1:c.2356_2358delinsATC	XP_011508661.1:p.Ile786=
XM_011510360.1:c.796_798delinsATC	XP_011508662.1:p.Ile266=
XM_011510361.1:c.787_789delinsATC	XP_011508663.1:p.Ile263=
XM_011510357.2:c.2866_2868delinsATC	XP_011508659.1:p.Ile956=
XM_011510358.2:c.2995_2997delinsATC	XP_011508660.1:p.Ile999=
XM_011510360.2:c.796_798delinsATC	XP_011508662.1:p.Ile266=
XM_011510361.2:c.787_789delinsATC	XP_011508663.1:p.Ile263=
XM_017004317.1:c.2995_2997delinsATC	XP_016859806.1:p.Ile999=
XM_024452961.1:c.2356_2358delinsATC	XP_024308729.1:p.Ile786=
NM_015909.4:c.2995_2997delinsATC MANE Select	NP_056993.2:p.Ile999=
NR_052013.3:n.3025_3027delinsATC