Canonical Allele Identifier: CA626340984

Gene: KANSL1

Linked Data

• dbSNP Id: rs2047378858
• gnomAD v2: 17-44269755-AAATG-A
• MyVariant Identifiers: chr17:g.44269756_44269759del (hg19) ; chr17:g.46192390_46192393del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46192392_46192395del , CM000679.2:g.46192392_46192395del	GRCh38
NC_000017.10:g.44269758_44269761del , CM000679.1:g.44269758_44269761del	GRCh37
NC_000017.9:g.41625535_41625538del	NCBI36
NG_032784.1:g.37982_37985del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.-90+430_-90+433del MANE Select	ENSP00000387393.3:n.-90+430_-90+433del
ENST00000571698.2:c.-90+1357_-90+1360del	ENSP00000459330.2:n.-90+1357_-90+1360del
ENST00000572904.6:c.-89-20161_-89-20158del	ENSP00000461484.1:n.-89-20161_-89-20158del
ENST00000574590.6:c.-89-20161_-89-20158del	ENSP00000461812.2:n.-89-20161_-89-20158del
ENST00000574655.6:n.166-20161_166-20158del
ENST00000575318.6:c.-89-20161_-89-20158del	ENSP00000461299.1:n.-89-20161_-89-20158del
ENST00000576739.2:c.-89-20161_-89-20158del	ENSP00000459627.1:n.-89-20161_-89-20158del
ENST00000638269.1:n.156-20161_156-20158del
ENST00000638275.1:c.-90+430_-90+433del	ENSP00000492576.1:n.-90+430_-90+433del
ENST00000638902.1:n.16-20161_16-20158del
ENST00000639099.1:n.162-20161_162-20158del
ENST00000639150.1:c.23+31278_23+31281del	ENSP00000491906.1:n.23+31278_23+31281del
ENST00000639356.1:n.162-20161_162-20158del
ENST00000639375.1:n.150-20161_150-20158del
ENST00000648792.1:c.-89-20161_-89-20158del	ENSP00000497628.1:n.-89-20161_-89-20158del
ENST00000262419.10:c.-90+26_-90+29del	ENSP00000262419.6:n.-90+26_-90+29del
ENST00000432791.5:c.-89-20161_-89-20158del	ENSP00000387393.2:n.-89-20161_-89-20158del
ENST00000571698.1:c.-90+1357_-90+1360del	ENSP00000459330.1:n.-90+1357_-90+1360del
ENST00000572904.5:c.-90+430_-90+433del	ENSP00000461484.1:n.-90+430_-90+433del
ENST00000574590.5:c.-89-20161_-89-20158del	ENSP00000461812.1:n.-89-20161_-89-20158del
ENST00000574655.5:c.-89-20161_-89-20158del	ENSP00000459359.1:n.-89-20161_-89-20158del
ENST00000576739.1:c.-89-20161_-89-20158del	ENSP00000459627.1:n.-89-20161_-89-20158del
NM_001193465.1:c.-89-20161_-89-20158del	NP_001180394.1:n.-89-20161_-89-20158del
NM_001193466.1:c.-90+26_-90+29del	NP_001180395.1:n.-90+26_-90+29del
NM_015443.3:c.-90+430_-90+433del	NP_056258.1:n.-90+430_-90+433del
XM_006721823.1:c.-89-20161_-89-20158del	XP_006721886.1:n.-89-20161_-89-20158del
XM_006721824.2:c.-89-20161_-89-20158del	XP_006721887.1:n.-89-20161_-89-20158del
XM_011524628.1:c.-89-20161_-89-20158del	XP_011522930.1:n.-89-20161_-89-20158del
XM_011524629.1:c.-89-20161_-89-20158del	XP_011522931.1:n.-89-20161_-89-20158del
XM_011524630.1:c.-89-20161_-89-20158del	XP_011522932.1:n.-89-20161_-89-20158del
XM_011524631.1:c.-89-20161_-89-20158del	XP_011522933.1:n.-89-20161_-89-20158del
XM_006721823.2:c.-89-20161_-89-20158del	XP_006721886.1:n.-89-20161_-89-20158del
XM_006721824.4:c.-89-20161_-89-20158del	XP_006721887.1:n.-89-20161_-89-20158del
XM_011524628.3:c.-89-20161_-89-20158del	XP_011522930.1:n.-89-20161_-89-20158del
XM_011524629.3:c.-89-20161_-89-20158del	XP_011522931.1:n.-89-20161_-89-20158del
XM_011524630.3:c.-89-20161_-89-20158del	XP_011522932.1:n.-89-20161_-89-20158del
XM_011524631.3:c.-89-20161_-89-20158del	XP_011522933.1:n.-89-20161_-89-20158del
XM_017024488.2:c.-89-20161_-89-20158del	XP_016879977.1:n.-89-20161_-89-20158del
XM_017024489.1:c.-90+430_-90+433del	XP_016879978.1:n.-90+430_-90+433del
NM_001193466.2:c.-90+26_-90+29del	NP_001180395.1:n.-90+26_-90+29del
NM_015443.4:c.-90+430_-90+433del MANE Select	NP_056258.1:n.-90+430_-90+433del
NM_001193465.2:c.-89-20161_-89-20158del	NP_001180394.1:n.-89-20161_-89-20158del
NM_001379198.1:c.-89-20161_-89-20158del	NP_001366127.1:n.-89-20161_-89-20158del