Canonical Allele Identifier: CA626341039

Gene: KANSL1

Linked Data

• dbSNP Id: rs1460003806
• gnomAD v2: 17-44270498-CCGGGAGGGCGGG-C
• gnomAD v3: 17-46193132-CCGGGAGGGCGGG-C
• gnomAD v4: 17-46193132-CCGGGAGGGCGGG-C
• MyVariant Identifiers: chr17:g.44270499_44270510del (hg19) ; chr17:g.46193133_46193144del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46193137_46193148del , CM000679.2:g.46193137_46193148del	GRCh38
NC_000017.10:g.44270503_44270514del , CM000679.1:g.44270503_44270514del	GRCh37
NC_000017.9:g.41626280_41626291del	NCBI36
NG_032784.1:g.37231_37242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.-411_-400del MANE Select	ENSP00000387393.3:n.-411_-400del
ENST00000571698.2:c.-90+606_-90+617del	ENSP00000459330.2:n.-90+606_-90+617del
ENST00000572904.6:c.-89-20912_-89-20901del	ENSP00000461484.1:n.-89-20912_-89-20901del
ENST00000574590.6:c.-89-20912_-89-20901del	ENSP00000461812.2:n.-89-20912_-89-20901del
ENST00000574655.6:n.166-20912_166-20901del
ENST00000575318.6:c.-89-20912_-89-20901del	ENSP00000461299.1:n.-89-20912_-89-20901del
ENST00000576739.2:c.-89-20912_-89-20901del	ENSP00000459627.1:n.-89-20912_-89-20901del
ENST00000638269.1:n.156-20912_156-20901del
ENST00000638275.1:c.-411_-400del	ENSP00000492576.1:n.-411_-400del
ENST00000638902.1:n.16-20912_16-20901del
ENST00000639099.1:n.162-20912_162-20901del
ENST00000639150.1:c.23+30527_23+30538del	ENSP00000491906.1:n.23+30527_23+30538del
ENST00000639356.1:n.162-20912_162-20901del
ENST00000639375.1:n.150-20912_150-20901del
ENST00000648792.1:c.-89-20912_-89-20901del	ENSP00000497628.1:n.-89-20912_-89-20901del
ENST00000432791.5:c.-89-20912_-89-20901del	ENSP00000387393.2:n.-89-20912_-89-20901del
ENST00000571698.1:c.-90+606_-90+617del	ENSP00000459330.1:n.-90+606_-90+617del
ENST00000574590.5:c.-89-20912_-89-20901del	ENSP00000461812.1:n.-89-20912_-89-20901del
ENST00000574655.5:c.-89-20912_-89-20901del	ENSP00000459359.1:n.-89-20912_-89-20901del
ENST00000576739.1:c.-89-20912_-89-20901del	ENSP00000459627.1:n.-89-20912_-89-20901del
NM_001193465.1:c.-89-20912_-89-20901del	NP_001180394.1:n.-89-20912_-89-20901del
XM_006721823.1:c.-89-20912_-89-20901del	XP_006721886.1:n.-89-20912_-89-20901del
XM_006721824.2:c.-89-20912_-89-20901del	XP_006721887.1:n.-89-20912_-89-20901del
XM_011524628.1:c.-89-20912_-89-20901del	XP_011522930.1:n.-89-20912_-89-20901del
XM_011524629.1:c.-89-20912_-89-20901del	XP_011522931.1:n.-89-20912_-89-20901del
XM_011524630.1:c.-89-20912_-89-20901del	XP_011522932.1:n.-89-20912_-89-20901del
XM_011524631.1:c.-89-20912_-89-20901del	XP_011522933.1:n.-89-20912_-89-20901del
XM_006721823.2:c.-89-20912_-89-20901del	XP_006721886.1:n.-89-20912_-89-20901del
XM_006721824.4:c.-89-20912_-89-20901del	XP_006721887.1:n.-89-20912_-89-20901del
XM_011524628.3:c.-89-20912_-89-20901del	XP_011522930.1:n.-89-20912_-89-20901del
XM_011524629.3:c.-89-20912_-89-20901del	XP_011522931.1:n.-89-20912_-89-20901del
XM_011524630.3:c.-89-20912_-89-20901del	XP_011522932.1:n.-89-20912_-89-20901del
XM_011524631.3:c.-89-20912_-89-20901del	XP_011522933.1:n.-89-20912_-89-20901del
XM_017024488.2:c.-89-20912_-89-20901del	XP_016879977.1:n.-89-20912_-89-20901del
NM_015443.4:c.-411_-400del MANE Select	NP_056258.1:n.-411_-400del
NM_001193465.2:c.-89-20912_-89-20901del	NP_001180394.1:n.-89-20912_-89-20901del
NM_001379198.1:c.-89-20912_-89-20901del	NP_001366127.1:n.-89-20912_-89-20901del