Canonical Allele Identifier: CA399986726

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44109520G>A (hg19) ; chr17:g.46032154G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46032154G>A , CM000679.2:g.46032154G>A	GRCh38
NC_000017.10:g.44109520G>A , CM000679.1:g.44109520G>A	GRCh37
NC_000017.9:g.41465367G>A	NCBI36
NG_032784.1:g.198221C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000432791.7:c.2983C>T MANE Select	ENSP00000387393.3:p.Pro995Ser
ENST00000572904.6:c.2983C>T	ENSP00000461484.1:p.Pro995Ser
ENST00000574590.6:c.2980C>T	ENSP00000461812.2:p.Pro994Ser
ENST00000575318.6:c.2791C>T	ENSP00000461299.1:p.Pro931Ser
ENST00000638275.1:c.2791C>T	ENSP00000492576.1:p.Pro931Ser
ENST00000639467.1:c.640C>T	ENSP00000492741.1:p.Pro214Ser
ENST00000639805.1:n.400C>T
ENST00000648792.1:c.2851C>T	ENSP00000497628.1:p.Pro951Ser
ENST00000262419.10:c.2983C>T	ENSP00000262419.6:p.Pro995Ser
ENST00000432791.5:c.2980C>T	ENSP00000387393.2:p.Pro994Ser
ENST00000572218.5:n.7200C>T
ENST00000572904.5:c.2983C>T	ENSP00000461484.1:p.Pro995Ser
ENST00000574590.5:c.2983C>T	ENSP00000461812.1:p.Pro995Ser
ENST00000574963.1:n.413C>T
ENST00000575318.5:c.2791C>T	ENSP00000461299.1:p.Pro931Ser
ENST00000576870.5:n.955C>T
NM_001193465.1:c.2980C>T	NP_001180394.1:p.Pro994Ser
NM_001193466.1:c.2983C>T	NP_001180395.1:p.Pro995Ser
NM_015443.3:c.2983C>T	NP_056258.1:p.Pro995Ser
XM_006721823.1:c.2983C>T	XP_006721886.1:p.Pro995Ser
XM_006721824.2:c.2983C>T	XP_006721887.1:p.Pro995Ser
XM_011524628.1:c.2980C>T	XP_011522930.1:p.Pro994Ser
XM_011524629.1:c.2881C>T	XP_011522931.1:p.Pro961Ser
XM_011524630.1:c.2794C>T	XP_011522932.1:p.Pro932Ser
XM_011524631.1:c.2791C>T	XP_011522933.1:p.Pro931Ser
XM_011524632.1:c.1753C>T	XP_011522934.1:p.Pro585Ser
XM_006721823.2:c.2983C>T	XP_006721886.1:p.Pro995Ser
XM_006721824.4:c.2983C>T	XP_006721887.1:p.Pro995Ser
XM_011524628.3:c.2980C>T	XP_011522930.1:p.Pro994Ser
XM_011524629.3:c.2881C>T	XP_011522931.1:p.Pro961Ser
XM_011524630.3:c.2794C>T	XP_011522932.1:p.Pro932Ser
XM_011524631.3:c.2791C>T	XP_011522933.1:p.Pro931Ser
XM_011524632.3:c.1753C>T	XP_011522934.1:p.Pro585Ser
XM_017024488.2:c.2791C>T	XP_016879977.1:p.Pro931Ser
NM_001193466.2:c.2983C>T	NP_001180395.1:p.Pro995Ser
NM_015443.4:c.2983C>T MANE Select	NP_056258.1:p.Pro995Ser
NM_001193465.2:c.2980C>T	NP_001180394.1:p.Pro994Ser
NM_001379198.1:c.2983C>T	NP_001366127.1:p.Pro995Ser