Canonical Allele Identifier: CA2638371409

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46031821-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031821_46031822insT , CM000679.2:g.46031821_46031822insT	GRCh38
NC_000017.10:g.44109187_44109188insT , CM000679.1:g.44109187_44109188insT	GRCh37
NC_000017.9:g.41465034_41465035insT	NCBI36
NG_032784.1:g.198553_198554insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3091-119_3091-118insA MANE Select	ENSP00000387393.3:n.3091-119_3091-118insA
ENST00000572904.6:c.3091-119_3091-118insA	ENSP00000461484.1:n.3091-119_3091-118insA
ENST00000574590.6:c.3088-119_3088-118insA	ENSP00000461812.2:n.3088-119_3088-118insA
ENST00000575318.6:c.2899-119_2899-118insA	ENSP00000461299.1:n.2899-119_2899-118insA
ENST00000638275.1:c.2899-119_2899-118insA	ENSP00000492576.1:n.2899-119_2899-118insA
ENST00000639805.1:n.508-119_508-118insA
ENST00000648792.1:c.2959-119_2959-118insA	ENSP00000497628.1:n.2959-119_2959-118insA
ENST00000262419.10:c.3091-119_3091-118insA	ENSP00000262419.6:n.3091-119_3091-118insA
ENST00000432791.5:c.3088-119_3088-118insA	ENSP00000387393.2:n.3088-119_3088-118insA
ENST00000572218.5:n.7308-119_7308-118insA
ENST00000572904.5:c.3091-119_3091-118insA	ENSP00000461484.1:n.3091-119_3091-118insA
ENST00000574590.5:c.3091-119_3091-118insA	ENSP00000461812.1:n.3091-119_3091-118insA
ENST00000574963.1:n.745_746insA
ENST00000575318.5:c.2899-119_2899-118insA	ENSP00000461299.1:n.2899-119_2899-118insA
ENST00000576870.5:n.1063-119_1063-118insA
NM_001193465.1:c.3088-119_3088-118insA	NP_001180394.1:n.3088-119_3088-118insA
NM_001193466.1:c.3091-119_3091-118insA	NP_001180395.1:n.3091-119_3091-118insA
NM_015443.3:c.3091-119_3091-118insA	NP_056258.1:n.3091-119_3091-118insA
XM_006721823.1:c.3091-119_3091-118insA	XP_006721886.1:n.3091-119_3091-118insA
XM_006721824.2:c.3091-119_3091-118insA	XP_006721887.1:n.3091-119_3091-118insA
XM_011524628.1:c.3088-119_3088-118insA	XP_011522930.1:n.3088-119_3088-118insA
XM_011524629.1:c.2989-119_2989-118insA	XP_011522931.1:n.2989-119_2989-118insA
XM_011524630.1:c.2902-119_2902-118insA	XP_011522932.1:n.2902-119_2902-118insA
XM_011524631.1:c.2899-119_2899-118insA	XP_011522933.1:n.2899-119_2899-118insA
XM_011524632.1:c.1861-119_1861-118insA	XP_011522934.1:n.1861-119_1861-118insA
XM_006721823.2:c.3091-119_3091-118insA	XP_006721886.1:n.3091-119_3091-118insA
XM_006721824.4:c.3091-119_3091-118insA	XP_006721887.1:n.3091-119_3091-118insA
XM_011524628.3:c.3088-119_3088-118insA	XP_011522930.1:n.3088-119_3088-118insA
XM_011524629.3:c.2989-119_2989-118insA	XP_011522931.1:n.2989-119_2989-118insA
XM_011524630.3:c.2902-119_2902-118insA	XP_011522932.1:n.2902-119_2902-118insA
XM_011524631.3:c.2899-119_2899-118insA	XP_011522933.1:n.2899-119_2899-118insA
XM_011524632.3:c.1861-119_1861-118insA	XP_011522934.1:n.1861-119_1861-118insA
XM_017024488.2:c.2899-119_2899-118insA	XP_016879977.1:n.2899-119_2899-118insA
NM_001193466.2:c.3091-119_3091-118insA	NP_001180395.1:n.3091-119_3091-118insA
NM_015443.4:c.3091-119_3091-118insA MANE Select	NP_056258.1:n.3091-119_3091-118insA
NM_001193465.2:c.3088-119_3088-118insA	NP_001180394.1:n.3088-119_3088-118insA
NM_001379198.1:c.3091-119_3091-118insA	NP_001366127.1:n.3091-119_3091-118insA