Canonical Allele Identifier: CA399980435

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44115999G>C (hg19) ; chr17:g.46038633G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46038633G>C , CM000679.2:g.46038633G>C	GRCh38
NC_000017.10:g.44115999G>C , CM000679.1:g.44115999G>C	GRCh37
NC_000017.9:g.41471846G>C	NCBI36
NG_032784.1:g.191742C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.2446C>G MANE Select	ENSP00000387393.3:p.His816Asp
ENST00000572904.6:c.2446C>G	ENSP00000461484.1:p.His816Asp
ENST00000573286.2:n.4129C>G
ENST00000574590.6:c.2446C>G	ENSP00000461812.2:p.His816Asp
ENST00000575318.6:c.2257C>G	ENSP00000461299.1:p.His753Asp
ENST00000576137.2:n.443C>G
ENST00000638275.1:c.2257C>G	ENSP00000492576.1:p.His753Asp
ENST00000639150.1:c.1180C>G	ENSP00000491906.1:p.His394Asp
ENST00000639467.1:c.109C>G	ENSP00000492741.1:p.His37Asp
ENST00000639531.1:c.2257C>G	ENSP00000491765.1:p.His753Asp
ENST00000640636.1:c.399C>G
ENST00000648792.1:c.2446C>G	ENSP00000497628.1:p.His816Asp
ENST00000262419.10:c.2446C>G	ENSP00000262419.6:p.His816Asp
ENST00000432791.5:c.2446C>G	ENSP00000387393.2:p.His816Asp
ENST00000572218.5:n.6663C>G
ENST00000572904.5:c.2446C>G	ENSP00000461484.1:p.His816Asp
ENST00000573286.1:n.302C>G
ENST00000574590.5:c.2446C>G	ENSP00000461812.1:p.His816Asp
ENST00000575318.5:c.2257C>G	ENSP00000461299.1:p.His753Asp
ENST00000576137.1:n.85C>G
ENST00000576870.5:n.418C>G
NM_001193465.1:c.2446C>G	NP_001180394.1:p.His816Asp
NM_001193466.1:c.2446C>G	NP_001180395.1:p.His816Asp
NM_015443.3:c.2446C>G	NP_056258.1:p.His816Asp
XM_006721823.1:c.2446C>G	XP_006721886.1:p.His816Asp
XM_006721824.2:c.2446C>G	XP_006721887.1:p.His816Asp
XM_011524628.1:c.2446C>G	XP_011522930.1:p.His816Asp
XM_011524629.1:c.2344C>G	XP_011522931.1:p.His782Asp
XM_011524630.1:c.2257C>G	XP_011522932.1:p.His753Asp
XM_011524631.1:c.2257C>G	XP_011522933.1:p.His753Asp
XM_011524632.1:c.1216C>G	XP_011522934.1:p.His406Asp
XM_006721823.2:c.2446C>G	XP_006721886.1:p.His816Asp
XM_006721824.4:c.2446C>G	XP_006721887.1:p.His816Asp
XM_011524628.3:c.2446C>G	XP_011522930.1:p.His816Asp
XM_011524629.3:c.2344C>G	XP_011522931.1:p.His782Asp
XM_011524630.3:c.2257C>G	XP_011522932.1:p.His753Asp
XM_011524631.3:c.2257C>G	XP_011522933.1:p.His753Asp
XM_011524632.3:c.1216C>G	XP_011522934.1:p.His406Asp
XM_017024488.2:c.2257C>G	XP_016879977.1:p.His753Asp
XM_017024489.1:c.2344C>G	XP_016879978.1:p.His782Asp
NM_001193466.2:c.2446C>G	NP_001180395.1:p.His816Asp
NM_015443.4:c.2446C>G MANE Select	NP_056258.1:p.His816Asp
NM_001193465.2:c.2446C>G	NP_001180394.1:p.His816Asp
NM_001379198.1:c.2446C>G	NP_001366127.1:p.His816Asp