Canonical Allele Identifier: CA399985378

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44108846C>A (hg19) ; chr17:g.46031480C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031480C>A , CM000679.2:g.46031480C>A	GRCh38
NC_000017.10:g.44108846C>A , CM000679.1:g.44108846C>A	GRCh37
NC_000017.9:g.41464693C>A	NCBI36
NG_032784.1:g.198895G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3314G>T MANE Select	ENSP00000387393.3:p.Arg1105Ile
ENST00000572904.6:c.3314G>T	ENSP00000461484.1:p.Arg1105Ile
ENST00000574590.6:c.3311G>T	ENSP00000461812.2:p.Arg1104Ile
ENST00000575318.6:c.3122G>T	ENSP00000461299.1:p.Arg1041Ile
ENST00000638275.1:c.3122G>T	ENSP00000492576.1:p.Arg1041Ile
ENST00000648792.1:c.3182G>T	ENSP00000497628.1:p.Arg1061Ile
ENST00000262419.10:c.3314G>T	ENSP00000262419.6:p.Arg1105Ile
ENST00000432791.5:c.3311G>T	ENSP00000387393.2:p.Arg1104Ile
ENST00000572218.5:n.7531G>T
ENST00000572904.5:c.3314G>T	ENSP00000461484.1:p.Arg1105Ile
ENST00000574590.5:c.3314G>T	ENSP00000461812.1:p.Arg1105Ile
ENST00000574963.1:n.1087G>T
ENST00000575318.5:c.3122G>T	ENSP00000461299.1:p.Arg1041Ile
ENST00000576870.5:n.1286G>T
NM_001193465.1:c.3311G>T	NP_001180394.1:p.Arg1104Ile
NM_001193466.1:c.3314G>T	NP_001180395.1:p.Arg1105Ile
NM_015443.3:c.3314G>T	NP_056258.1:p.Arg1105Ile
XM_006721823.1:c.3314G>T	XP_006721886.1:p.Arg1105Ile
XM_006721824.2:c.3314G>T	XP_006721887.1:p.Arg1105Ile
XM_011524628.1:c.3311G>T	XP_011522930.1:p.Arg1104Ile
XM_011524629.1:c.3212G>T	XP_011522931.1:p.Arg1071Ile
XM_011524630.1:c.3125G>T	XP_011522932.1:p.Arg1042Ile
XM_011524631.1:c.3122G>T	XP_011522933.1:p.Arg1041Ile
XM_011524632.1:c.2084G>T	XP_011522934.1:p.Arg695Ile
XM_006721823.2:c.3314G>T	XP_006721886.1:p.Arg1105Ile
XM_006721824.4:c.3314G>T	XP_006721887.1:p.Arg1105Ile
XM_011524628.3:c.3311G>T	XP_011522930.1:p.Arg1104Ile
XM_011524629.3:c.3212G>T	XP_011522931.1:p.Arg1071Ile
XM_011524630.3:c.3125G>T	XP_011522932.1:p.Arg1042Ile
XM_011524631.3:c.3122G>T	XP_011522933.1:p.Arg1041Ile
XM_011524632.3:c.2084G>T	XP_011522934.1:p.Arg695Ile
XM_017024488.2:c.3122G>T	XP_016879977.1:p.Arg1041Ile
NM_001193466.2:c.3314G>T	NP_001180395.1:p.Arg1105Ile
NM_015443.4:c.3314G>T MANE Select	NP_056258.1:p.Arg1105Ile
NM_001193465.2:c.3311G>T	NP_001180394.1:p.Arg1104Ile
NM_001379198.1:c.3314G>T	NP_001366127.1:p.Arg1105Ile