Canonical Allele Identifier: CA500371726

Gene: KANSL1

Linked Data

• dbSNP Id: rs1568365402
• gnomAD v4: 17-46031680-C-G
• MyVariant Identifiers: chr17:g.44109046C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031680C>G , CM000679.2:g.46031680C>G	GRCh38
NC_000017.10:g.44109046C>G , CM000679.1:g.44109046C>G	GRCh37
NC_000017.9:g.41464893C>G	NCBI36
NG_032784.1:g.198695G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3114G>C MANE Select	ENSP00000387393.3:p.Arg1038=
ENST00000572904.6:c.3114G>C	ENSP00000461484.1:p.Arg1038=
ENST00000574590.6:c.3111G>C	ENSP00000461812.2:p.Arg1037=
ENST00000575318.6:c.2922G>C	ENSP00000461299.1:p.Arg974=
ENST00000638275.1:c.2922G>C	ENSP00000492576.1:p.Arg974=
ENST00000639805.1:n.531G>C
ENST00000648792.1:c.2982G>C	ENSP00000497628.1:p.Arg994=
ENST00000262419.10:c.3114G>C	ENSP00000262419.6:p.Arg1038=
ENST00000432791.5:c.3111G>C	ENSP00000387393.2:p.Arg1037=
ENST00000572218.5:n.7331G>C
ENST00000572904.5:c.3114G>C	ENSP00000461484.1:p.Arg1038=
ENST00000574590.5:c.3114G>C	ENSP00000461812.1:p.Arg1038=
ENST00000574963.1:n.887G>C
ENST00000575318.5:c.2922G>C	ENSP00000461299.1:p.Arg974=
ENST00000576870.5:n.1086G>C
NM_001193465.1:c.3111G>C	NP_001180394.1:p.Arg1037=
NM_001193466.1:c.3114G>C	NP_001180395.1:p.Arg1038=
NM_015443.3:c.3114G>C	NP_056258.1:p.Arg1038=
XM_006721823.1:c.3114G>C	XP_006721886.1:p.Arg1038=
XM_006721824.2:c.3114G>C	XP_006721887.1:p.Arg1038=
XM_011524628.1:c.3111G>C	XP_011522930.1:p.Arg1037=
XM_011524629.1:c.3012G>C	XP_011522931.1:p.Arg1004=
XM_011524630.1:c.2925G>C	XP_011522932.1:p.Arg975=
XM_011524631.1:c.2922G>C	XP_011522933.1:p.Arg974=
XM_011524632.1:c.1884G>C	XP_011522934.1:p.Arg628=
XM_006721823.2:c.3114G>C	XP_006721886.1:p.Arg1038=
XM_006721824.4:c.3114G>C	XP_006721887.1:p.Arg1038=
XM_011524628.3:c.3111G>C	XP_011522930.1:p.Arg1037=
XM_011524629.3:c.3012G>C	XP_011522931.1:p.Arg1004=
XM_011524630.3:c.2925G>C	XP_011522932.1:p.Arg975=
XM_011524631.3:c.2922G>C	XP_011522933.1:p.Arg974=
XM_011524632.3:c.1884G>C	XP_011522934.1:p.Arg628=
XM_017024488.2:c.2922G>C	XP_016879977.1:p.Arg974=
NM_001193466.2:c.3114G>C	NP_001180395.1:p.Arg1038=
NM_015443.4:c.3114G>C MANE Select	NP_056258.1:p.Arg1038=
NM_001193465.2:c.3111G>C	NP_001180394.1:p.Arg1037=
NM_001379198.1:c.3114G>C	NP_001366127.1:p.Arg1038=