Canonical Allele Identifier: CA399987250

Gene: KANSL1

Linked Data

• ClinVar Variation Id: 2896683
• ClinVar RCV Id: RCV003642629
• dbSNP Id: rs2077031570
• gnomAD v3: 17-46032247-G-A
• gnomAD v4: 17-46032247-G-A
• MyVariant Identifiers: chr17:g.44109613G>A (hg19) ; chr17:g.46032247G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032247G>A , CM000679.2:g.46032247G>A	GRCh38
NC_000017.10:g.44109613G>A , CM000679.1:g.44109613G>A	GRCh37
NC_000017.9:g.41465460G>A	NCBI36
NG_032784.1:g.198128C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.2890C>T MANE Select	ENSP00000387393.3:p.Pro964Ser
ENST00000572904.6:c.2890C>T	ENSP00000461484.1:p.Pro964Ser
ENST00000574590.6:c.2887C>T	ENSP00000461812.2:p.Pro963Ser
ENST00000575318.6:c.2698C>T	ENSP00000461299.1:p.Pro900Ser
ENST00000638275.1:c.2698C>T	ENSP00000492576.1:p.Pro900Ser
ENST00000638291.1:n.718C>T
ENST00000638551.1:n.838C>T
ENST00000639467.1:c.547C>T	ENSP00000492741.1:p.Pro183Ser
ENST00000639805.1:n.307C>T
ENST00000648792.1:c.2838-80C>T	ENSP00000497628.1:n.2838-80C>T
ENST00000262419.10:c.2890C>T	ENSP00000262419.6:p.Pro964Ser
ENST00000432791.5:c.2887C>T	ENSP00000387393.2:p.Pro963Ser
ENST00000572218.5:n.7107C>T
ENST00000572904.5:c.2890C>T	ENSP00000461484.1:p.Pro964Ser
ENST00000573682.1:n.276C>T
ENST00000574590.5:c.2890C>T	ENSP00000461812.1:p.Pro964Ser
ENST00000574963.1:n.320C>T
ENST00000575318.5:c.2698C>T	ENSP00000461299.1:p.Pro900Ser
ENST00000576870.5:n.862C>T
NM_001193465.1:c.2887C>T	NP_001180394.1:p.Pro963Ser
NM_001193466.1:c.2890C>T	NP_001180395.1:p.Pro964Ser
NM_015443.3:c.2890C>T	NP_056258.1:p.Pro964Ser
XM_006721823.1:c.2890C>T	XP_006721886.1:p.Pro964Ser
XM_006721824.2:c.2890C>T	XP_006721887.1:p.Pro964Ser
XM_011524628.1:c.2887C>T	XP_011522930.1:p.Pro963Ser
XM_011524629.1:c.2788C>T	XP_011522931.1:p.Pro930Ser
XM_011524630.1:c.2701C>T	XP_011522932.1:p.Pro901Ser
XM_011524631.1:c.2698C>T	XP_011522933.1:p.Pro900Ser
XM_011524632.1:c.1660C>T	XP_011522934.1:p.Pro554Ser
XM_006721823.2:c.2890C>T	XP_006721886.1:p.Pro964Ser
XM_006721824.4:c.2890C>T	XP_006721887.1:p.Pro964Ser
XM_011524628.3:c.2887C>T	XP_011522930.1:p.Pro963Ser
XM_011524629.3:c.2788C>T	XP_011522931.1:p.Pro930Ser
XM_011524630.3:c.2701C>T	XP_011522932.1:p.Pro901Ser
XM_011524631.3:c.2698C>T	XP_011522933.1:p.Pro900Ser
XM_011524632.3:c.1660C>T	XP_011522934.1:p.Pro554Ser
XM_017024488.2:c.2698C>T	XP_016879977.1:p.Pro900Ser
NM_001193466.2:c.2890C>T	NP_001180395.1:p.Pro964Ser
NM_015443.4:c.2890C>T MANE Select	NP_056258.1:p.Pro964Ser
NM_001193465.2:c.2887C>T	NP_001180394.1:p.Pro963Ser
NM_001379198.1:c.2890C>T	NP_001366127.1:p.Pro964Ser