Canonical Allele Identifier: CA399985790

Gene: KANSL1

Linked Data

• MyVariant Identifiers: chr17:g.44108928C>A (hg19) ; chr17:g.46031562C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46031562C>A , CM000679.2:g.46031562C>A	GRCh38
NC_000017.10:g.44108928C>A , CM000679.1:g.44108928C>A	GRCh37
NC_000017.9:g.41464775C>A	NCBI36
NG_032784.1:g.198813G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.3232G>T MANE Select	ENSP00000387393.3:p.Ala1078Ser
ENST00000572904.6:c.3232G>T	ENSP00000461484.1:p.Ala1078Ser
ENST00000574590.6:c.3229G>T	ENSP00000461812.2:p.Ala1077Ser
ENST00000575318.6:c.3040G>T	ENSP00000461299.1:p.Ala1014Ser
ENST00000638275.1:c.3040G>T	ENSP00000492576.1:p.Ala1014Ser
ENST00000648792.1:c.3100G>T	ENSP00000497628.1:p.Ala1034Ser
ENST00000262419.10:c.3232G>T	ENSP00000262419.6:p.Ala1078Ser
ENST00000432791.5:c.3229G>T	ENSP00000387393.2:p.Ala1077Ser
ENST00000572218.5:n.7449G>T
ENST00000572904.5:c.3232G>T	ENSP00000461484.1:p.Ala1078Ser
ENST00000574590.5:c.3232G>T	ENSP00000461812.1:p.Ala1078Ser
ENST00000574963.1:n.1005G>T
ENST00000575318.5:c.3040G>T	ENSP00000461299.1:p.Ala1014Ser
ENST00000576870.5:n.1204G>T
NM_001193465.1:c.3229G>T	NP_001180394.1:p.Ala1077Ser
NM_001193466.1:c.3232G>T	NP_001180395.1:p.Ala1078Ser
NM_015443.3:c.3232G>T	NP_056258.1:p.Ala1078Ser
XM_006721823.1:c.3232G>T	XP_006721886.1:p.Ala1078Ser
XM_006721824.2:c.3232G>T	XP_006721887.1:p.Ala1078Ser
XM_011524628.1:c.3229G>T	XP_011522930.1:p.Ala1077Ser
XM_011524629.1:c.3130G>T	XP_011522931.1:p.Ala1044Ser
XM_011524630.1:c.3043G>T	XP_011522932.1:p.Ala1015Ser
XM_011524631.1:c.3040G>T	XP_011522933.1:p.Ala1014Ser
XM_011524632.1:c.2002G>T	XP_011522934.1:p.Ala668Ser
XM_006721823.2:c.3232G>T	XP_006721886.1:p.Ala1078Ser
XM_006721824.4:c.3232G>T	XP_006721887.1:p.Ala1078Ser
XM_011524628.3:c.3229G>T	XP_011522930.1:p.Ala1077Ser
XM_011524629.3:c.3130G>T	XP_011522931.1:p.Ala1044Ser
XM_011524630.3:c.3043G>T	XP_011522932.1:p.Ala1015Ser
XM_011524631.3:c.3040G>T	XP_011522933.1:p.Ala1014Ser
XM_011524632.3:c.2002G>T	XP_011522934.1:p.Ala668Ser
XM_017024488.2:c.3040G>T	XP_016879977.1:p.Ala1014Ser
NM_001193466.2:c.3232G>T	NP_001180395.1:p.Ala1078Ser
NM_015443.4:c.3232G>T MANE Select	NP_056258.1:p.Ala1078Ser
NM_001193465.2:c.3229G>T	NP_001180394.1:p.Ala1077Ser
NM_001379198.1:c.3232G>T	NP_001366127.1:p.Ala1078Ser