Canonical Allele Identifier: CA399987303

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44109634G>T (hg19) ; chr17:g.46032268G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032268G>T , CM000679.2:g.46032268G>T	GRCh38
NC_000017.10:g.44109634G>T , CM000679.1:g.44109634G>T	GRCh37
NC_000017.9:g.41465481G>T	NCBI36
NG_032784.1:g.198107C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2869C>A MANE Select	ENSP00000387393.3:p.Pro957Thr
ENST00000572904.6:c.2869C>A	ENSP00000461484.1:p.Pro957Thr
ENST00000574590.6:c.2866C>A	ENSP00000461812.2:p.Pro956Thr
ENST00000575318.6:c.2677C>A	ENSP00000461299.1:p.Pro893Thr
ENST00000638275.1:c.2677C>A	ENSP00000492576.1:p.Pro893Thr
ENST00000638291.1:n.697C>A
ENST00000638551.1:n.817C>A
ENST00000639467.1:c.526C>A	ENSP00000492741.1:p.Pro176Thr
ENST00000639531.1:c.2680C>A	ENSP00000491765.1:p.Pro894Thr
ENST00000639805.1:n.286C>A
ENST00000640751.1:n.464C>A
ENST00000648792.1:c.2838-101C>A	ENSP00000497628.1:n.2838-101C>A
ENST00000262419.10:c.2869C>A	ENSP00000262419.6:p.Pro957Thr
ENST00000432791.5:c.2866C>A	ENSP00000387393.2:p.Pro956Thr
ENST00000572218.5:n.7086C>A
ENST00000572904.5:c.2869C>A	ENSP00000461484.1:p.Pro957Thr
ENST00000573682.1:n.255C>A
ENST00000574590.5:c.2869C>A	ENSP00000461812.1:p.Pro957Thr
ENST00000574963.1:n.299C>A
ENST00000575318.5:c.2677C>A	ENSP00000461299.1:p.Pro893Thr
ENST00000576870.5:n.841C>A
NM_001193465.1:c.2866C>A	NP_001180394.1:p.Pro956Thr
NM_001193466.1:c.2869C>A	NP_001180395.1:p.Pro957Thr
NM_015443.3:c.2869C>A	NP_056258.1:p.Pro957Thr
XM_006721823.1:c.2869C>A	XP_006721886.1:p.Pro957Thr
XM_006721824.2:c.2869C>A	XP_006721887.1:p.Pro957Thr
XM_011524628.1:c.2866C>A	XP_011522930.1:p.Pro956Thr
XM_011524629.1:c.2767C>A	XP_011522931.1:p.Pro923Thr
XM_011524630.1:c.2680C>A	XP_011522932.1:p.Pro894Thr
XM_011524631.1:c.2677C>A	XP_011522933.1:p.Pro893Thr
XM_011524632.1:c.1639C>A	XP_011522934.1:p.Pro547Thr
XM_006721823.2:c.2869C>A	XP_006721886.1:p.Pro957Thr
XM_006721824.4:c.2869C>A	XP_006721887.1:p.Pro957Thr
XM_011524628.3:c.2866C>A	XP_011522930.1:p.Pro956Thr
XM_011524629.3:c.2767C>A	XP_011522931.1:p.Pro923Thr
XM_011524630.3:c.2680C>A	XP_011522932.1:p.Pro894Thr
XM_011524631.3:c.2677C>A	XP_011522933.1:p.Pro893Thr
XM_011524632.3:c.1639C>A	XP_011522934.1:p.Pro547Thr
XM_017024488.2:c.2677C>A	XP_016879977.1:p.Pro893Thr
NM_001193466.2:c.2869C>A	NP_001180395.1:p.Pro957Thr
NM_015443.4:c.2869C>A MANE Select	NP_056258.1:p.Pro957Thr
NM_001193465.2:c.2866C>A	NP_001180394.1:p.Pro956Thr
NM_001379198.1:c.2869C>A	NP_001366127.1:p.Pro957Thr