Canonical Allele Identifier: CA399985589

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46031520-G-C
• MyVariant Identifiers: chr17:g.44108886G>C (hg19) ; chr17:g.46031520G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031520G>C , CM000679.2:g.46031520G>C	GRCh38
NC_000017.10:g.44108886G>C , CM000679.1:g.44108886G>C	GRCh37
NC_000017.9:g.41464733G>C	NCBI36
NG_032784.1:g.198855C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3274C>G MANE Select	ENSP00000387393.3:p.His1092Asp
ENST00000572904.6:c.3274C>G	ENSP00000461484.1:p.His1092Asp
ENST00000574590.6:c.3271C>G	ENSP00000461812.2:p.His1091Asp
ENST00000575318.6:c.3082C>G	ENSP00000461299.1:p.His1028Asp
ENST00000638275.1:c.3082C>G	ENSP00000492576.1:p.His1028Asp
ENST00000648792.1:c.3142C>G	ENSP00000497628.1:p.His1048Asp
ENST00000262419.10:c.3274C>G	ENSP00000262419.6:p.His1092Asp
ENST00000432791.5:c.3271C>G	ENSP00000387393.2:p.His1091Asp
ENST00000572218.5:n.7491C>G
ENST00000572904.5:c.3274C>G	ENSP00000461484.1:p.His1092Asp
ENST00000574590.5:c.3274C>G	ENSP00000461812.1:p.His1092Asp
ENST00000574963.1:n.1047C>G
ENST00000575318.5:c.3082C>G	ENSP00000461299.1:p.His1028Asp
ENST00000576870.5:n.1246C>G
NM_001193465.1:c.3271C>G	NP_001180394.1:p.His1091Asp
NM_001193466.1:c.3274C>G	NP_001180395.1:p.His1092Asp
NM_015443.3:c.3274C>G	NP_056258.1:p.His1092Asp
XM_006721823.1:c.3274C>G	XP_006721886.1:p.His1092Asp
XM_006721824.2:c.3274C>G	XP_006721887.1:p.His1092Asp
XM_011524628.1:c.3271C>G	XP_011522930.1:p.His1091Asp
XM_011524629.1:c.3172C>G	XP_011522931.1:p.His1058Asp
XM_011524630.1:c.3085C>G	XP_011522932.1:p.His1029Asp
XM_011524631.1:c.3082C>G	XP_011522933.1:p.His1028Asp
XM_011524632.1:c.2044C>G	XP_011522934.1:p.His682Asp
XM_006721823.2:c.3274C>G	XP_006721886.1:p.His1092Asp
XM_006721824.4:c.3274C>G	XP_006721887.1:p.His1092Asp
XM_011524628.3:c.3271C>G	XP_011522930.1:p.His1091Asp
XM_011524629.3:c.3172C>G	XP_011522931.1:p.His1058Asp
XM_011524630.3:c.3085C>G	XP_011522932.1:p.His1029Asp
XM_011524631.3:c.3082C>G	XP_011522933.1:p.His1028Asp
XM_011524632.3:c.2044C>G	XP_011522934.1:p.His682Asp
XM_017024488.2:c.3082C>G	XP_016879977.1:p.His1028Asp
NM_001193466.2:c.3274C>G	NP_001180395.1:p.His1092Asp
NM_015443.4:c.3274C>G MANE Select	NP_056258.1:p.His1092Asp
NM_001193465.2:c.3271C>G	NP_001180394.1:p.His1091Asp
NM_001379198.1:c.3274C>G	NP_001366127.1:p.His1092Asp