Canonical Allele Identifier: CA399987307

Gene: KANSL1

Linked Data

• gnomAD v4: 17-46032270-G-C
• MyVariant Identifiers: chr17:g.44109636G>C (hg19) ; chr17:g.46032270G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032270G>C , CM000679.2:g.46032270G>C	GRCh38
NC_000017.10:g.44109636G>C , CM000679.1:g.44109636G>C	GRCh37
NC_000017.9:g.41465483G>C	NCBI36
NG_032784.1:g.198105C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2867C>G MANE Select	ENSP00000387393.3:p.Thr956Ser
ENST00000572904.6:c.2867C>G	ENSP00000461484.1:p.Thr956Ser
ENST00000574590.6:c.2864C>G	ENSP00000461812.2:p.Thr955Ser
ENST00000575318.6:c.2675C>G	ENSP00000461299.1:p.Thr892Ser
ENST00000638275.1:c.2675C>G	ENSP00000492576.1:p.Thr892Ser
ENST00000638291.1:n.695C>G
ENST00000638551.1:n.815C>G
ENST00000639467.1:c.524C>G	ENSP00000492741.1:p.Thr175Ser
ENST00000639531.1:c.2678C>G	ENSP00000491765.1:p.Thr893Ser
ENST00000639805.1:n.284C>G
ENST00000640751.1:n.462C>G
ENST00000648792.1:c.2838-103C>G	ENSP00000497628.1:n.2838-103C>G
ENST00000262419.10:c.2867C>G	ENSP00000262419.6:p.Thr956Ser
ENST00000432791.5:c.2864C>G	ENSP00000387393.2:p.Thr955Ser
ENST00000572218.5:n.7084C>G
ENST00000572904.5:c.2867C>G	ENSP00000461484.1:p.Thr956Ser
ENST00000573682.1:n.253C>G
ENST00000574590.5:c.2867C>G	ENSP00000461812.1:p.Thr956Ser
ENST00000574963.1:n.297C>G
ENST00000575318.5:c.2675C>G	ENSP00000461299.1:p.Thr892Ser
ENST00000576870.5:n.839C>G
NM_001193465.1:c.2864C>G	NP_001180394.1:p.Thr955Ser
NM_001193466.1:c.2867C>G	NP_001180395.1:p.Thr956Ser
NM_015443.3:c.2867C>G	NP_056258.1:p.Thr956Ser
XM_006721823.1:c.2867C>G	XP_006721886.1:p.Thr956Ser
XM_006721824.2:c.2867C>G	XP_006721887.1:p.Thr956Ser
XM_011524628.1:c.2864C>G	XP_011522930.1:p.Thr955Ser
XM_011524629.1:c.2765C>G	XP_011522931.1:p.Thr922Ser
XM_011524630.1:c.2678C>G	XP_011522932.1:p.Thr893Ser
XM_011524631.1:c.2675C>G	XP_011522933.1:p.Thr892Ser
XM_011524632.1:c.1637C>G	XP_011522934.1:p.Thr546Ser
XM_006721823.2:c.2867C>G	XP_006721886.1:p.Thr956Ser
XM_006721824.4:c.2867C>G	XP_006721887.1:p.Thr956Ser
XM_011524628.3:c.2864C>G	XP_011522930.1:p.Thr955Ser
XM_011524629.3:c.2765C>G	XP_011522931.1:p.Thr922Ser
XM_011524630.3:c.2678C>G	XP_011522932.1:p.Thr893Ser
XM_011524631.3:c.2675C>G	XP_011522933.1:p.Thr892Ser
XM_011524632.3:c.1637C>G	XP_011522934.1:p.Thr546Ser
XM_017024488.2:c.2675C>G	XP_016879977.1:p.Thr892Ser
NM_001193466.2:c.2867C>G	NP_001180395.1:p.Thr956Ser
NM_015443.4:c.2867C>G MANE Select	NP_056258.1:p.Thr956Ser
NM_001193465.2:c.2864C>G	NP_001180394.1:p.Thr955Ser
NM_001379198.1:c.2867C>G	NP_001366127.1:p.Thr956Ser