Canonical Allele Identifier: CA2638371248

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46031760-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031761_46031762del , CM000679.2:g.46031761_46031762del	GRCh38
NC_000017.10:g.44109127_44109128del , CM000679.1:g.44109127_44109128del	GRCh37
NC_000017.9:g.41464974_41464975del	NCBI36
NG_032784.1:g.198613_198614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3091-59_3091-58del MANE Select	ENSP00000387393.3:n.3091-59_3091-58del
ENST00000572904.6:c.3091-59_3091-58del	ENSP00000461484.1:n.3091-59_3091-58del
ENST00000574590.6:c.3088-59_3088-58del	ENSP00000461812.2:n.3088-59_3088-58del
ENST00000575318.6:c.2899-59_2899-58del	ENSP00000461299.1:n.2899-59_2899-58del
ENST00000638275.1:c.2899-59_2899-58del	ENSP00000492576.1:n.2899-59_2899-58del
ENST00000639805.1:n.508-59_508-58del
ENST00000648792.1:c.2959-59_2959-58del	ENSP00000497628.1:n.2959-59_2959-58del
ENST00000262419.10:c.3091-59_3091-58del	ENSP00000262419.6:n.3091-59_3091-58del
ENST00000432791.5:c.3088-59_3088-58del	ENSP00000387393.2:n.3088-59_3088-58del
ENST00000572218.5:n.7308-59_7308-58del
ENST00000572904.5:c.3091-59_3091-58del	ENSP00000461484.1:n.3091-59_3091-58del
ENST00000574590.5:c.3091-59_3091-58del	ENSP00000461812.1:n.3091-59_3091-58del
ENST00000574963.1:n.805_806del
ENST00000575318.5:c.2899-59_2899-58del	ENSP00000461299.1:n.2899-59_2899-58del
ENST00000576870.5:n.1063-59_1063-58del
NM_001193465.1:c.3088-59_3088-58del	NP_001180394.1:n.3088-59_3088-58del
NM_001193466.1:c.3091-59_3091-58del	NP_001180395.1:n.3091-59_3091-58del
NM_015443.3:c.3091-59_3091-58del	NP_056258.1:n.3091-59_3091-58del
XM_006721823.1:c.3091-59_3091-58del	XP_006721886.1:n.3091-59_3091-58del
XM_006721824.2:c.3091-59_3091-58del	XP_006721887.1:n.3091-59_3091-58del
XM_011524628.1:c.3088-59_3088-58del	XP_011522930.1:n.3088-59_3088-58del
XM_011524629.1:c.2989-59_2989-58del	XP_011522931.1:n.2989-59_2989-58del
XM_011524630.1:c.2902-59_2902-58del	XP_011522932.1:n.2902-59_2902-58del
XM_011524631.1:c.2899-59_2899-58del	XP_011522933.1:n.2899-59_2899-58del
XM_011524632.1:c.1861-59_1861-58del	XP_011522934.1:n.1861-59_1861-58del
XM_006721823.2:c.3091-59_3091-58del	XP_006721886.1:n.3091-59_3091-58del
XM_006721824.4:c.3091-59_3091-58del	XP_006721887.1:n.3091-59_3091-58del
XM_011524628.3:c.3088-59_3088-58del	XP_011522930.1:n.3088-59_3088-58del
XM_011524629.3:c.2989-59_2989-58del	XP_011522931.1:n.2989-59_2989-58del
XM_011524630.3:c.2902-59_2902-58del	XP_011522932.1:n.2902-59_2902-58del
XM_011524631.3:c.2899-59_2899-58del	XP_011522933.1:n.2899-59_2899-58del
XM_011524632.3:c.1861-59_1861-58del	XP_011522934.1:n.1861-59_1861-58del
XM_017024488.2:c.2899-59_2899-58del	XP_016879977.1:n.2899-59_2899-58del
NM_001193466.2:c.3091-59_3091-58del	NP_001180395.1:n.3091-59_3091-58del
NM_015443.4:c.3091-59_3091-58del MANE Select	NP_056258.1:n.3091-59_3091-58del
NM_001193465.2:c.3088-59_3088-58del	NP_001180394.1:n.3088-59_3088-58del
NM_001379198.1:c.3091-59_3091-58del	NP_001366127.1:n.3091-59_3091-58del