Canonical Allele Identifier: CA399987167

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44109589G>T (hg19) ; chr17:g.46032223G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032223G>T , CM000679.2:g.46032223G>T	GRCh38
NC_000017.10:g.44109589G>T , CM000679.1:g.44109589G>T	GRCh37
NC_000017.9:g.41465436G>T	NCBI36
NG_032784.1:g.198152C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2914C>A MANE Select	ENSP00000387393.3:p.Pro972Thr
ENST00000572904.6:c.2914C>A	ENSP00000461484.1:p.Pro972Thr
ENST00000574590.6:c.2911C>A	ENSP00000461812.2:p.Pro971Thr
ENST00000575318.6:c.2722C>A	ENSP00000461299.1:p.Pro908Thr
ENST00000638275.1:c.2722C>A	ENSP00000492576.1:p.Pro908Thr
ENST00000638291.1:n.742C>A
ENST00000638551.1:n.862C>A
ENST00000639467.1:c.571C>A	ENSP00000492741.1:p.Pro191Thr
ENST00000639805.1:n.331C>A
ENST00000648792.1:c.2838-56C>A	ENSP00000497628.1:n.2838-56C>A
ENST00000262419.10:c.2914C>A	ENSP00000262419.6:p.Pro972Thr
ENST00000432791.5:c.2911C>A	ENSP00000387393.2:p.Pro971Thr
ENST00000572218.5:n.7131C>A
ENST00000572904.5:c.2914C>A	ENSP00000461484.1:p.Pro972Thr
ENST00000573682.1:n.300C>A
ENST00000574590.5:c.2914C>A	ENSP00000461812.1:p.Pro972Thr
ENST00000574963.1:n.344C>A
ENST00000575318.5:c.2722C>A	ENSP00000461299.1:p.Pro908Thr
ENST00000576870.5:n.886C>A
NM_001193465.1:c.2911C>A	NP_001180394.1:p.Pro971Thr
NM_001193466.1:c.2914C>A	NP_001180395.1:p.Pro972Thr
NM_015443.3:c.2914C>A	NP_056258.1:p.Pro972Thr
XM_006721823.1:c.2914C>A	XP_006721886.1:p.Pro972Thr
XM_006721824.2:c.2914C>A	XP_006721887.1:p.Pro972Thr
XM_011524628.1:c.2911C>A	XP_011522930.1:p.Pro971Thr
XM_011524629.1:c.2812C>A	XP_011522931.1:p.Pro938Thr
XM_011524630.1:c.2725C>A	XP_011522932.1:p.Pro909Thr
XM_011524631.1:c.2722C>A	XP_011522933.1:p.Pro908Thr
XM_011524632.1:c.1684C>A	XP_011522934.1:p.Pro562Thr
XM_006721823.2:c.2914C>A	XP_006721886.1:p.Pro972Thr
XM_006721824.4:c.2914C>A	XP_006721887.1:p.Pro972Thr
XM_011524628.3:c.2911C>A	XP_011522930.1:p.Pro971Thr
XM_011524629.3:c.2812C>A	XP_011522931.1:p.Pro938Thr
XM_011524630.3:c.2725C>A	XP_011522932.1:p.Pro909Thr
XM_011524631.3:c.2722C>A	XP_011522933.1:p.Pro908Thr
XM_011524632.3:c.1684C>A	XP_011522934.1:p.Pro562Thr
XM_017024488.2:c.2722C>A	XP_016879977.1:p.Pro908Thr
NM_001193466.2:c.2914C>A	NP_001180395.1:p.Pro972Thr
NM_015443.4:c.2914C>A MANE Select	NP_056258.1:p.Pro972Thr
NM_001193465.2:c.2911C>A	NP_001180394.1:p.Pro971Thr
NM_001379198.1:c.2914C>A	NP_001366127.1:p.Pro972Thr