Canonical Allele Identifier: CA2262179928

Gene: KANSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46171267_46171268delinsCA , CM000679.2:g.46171267_46171268delinsCA	GRCh38
NC_000017.10:g.44248633_44248634delinsCA , CM000679.1:g.44248633_44248634delinsCA	GRCh37
NC_000017.9:g.41604410_41604411delinsCA	NCBI36
NG_032784.1:g.59107_59108delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432791.7:c.876_877delinsTG MANE Select	ENSP00000387393.3:p.Ala292=
ENST00000571698.2:c.876_877delinsTG	ENSP00000459330.2:p.Ala292=
ENST00000572904.6:c.876_877delinsTG	ENSP00000461484.1:p.Ala292=
ENST00000574590.6:c.876_877delinsTG	ENSP00000461812.2:p.Ala292=
ENST00000574655.6:n.1130_1131delinsTG
ENST00000575318.6:c.876_877delinsTG	ENSP00000461299.1:p.Ala292=
ENST00000638269.1:n.1120_1121delinsTG
ENST00000638275.1:c.876_877delinsTG	ENSP00000492576.1:p.Ala292=
ENST00000638902.1:n.980_981delinsTG
ENST00000639099.1:n.1126_1127delinsTG
ENST00000639150.1:c.23+52403_23+52404delinsTG	ENSP00000491906.1:n.23+52403_23+52404delinsTG
ENST00000639356.1:n.1126_1127delinsTG
ENST00000639375.1:n.1114_1115delinsTG
ENST00000639531.1:c.876_877delinsTG	ENSP00000491765.1:p.Ala292=
ENST00000639853.1:c.149_150delinsTG
ENST00000648792.1:c.876_877delinsTG	ENSP00000497628.1:p.Ala292=
ENST00000262419.10:c.876_877delinsTG	ENSP00000262419.6:p.Ala292=
ENST00000432791.5:c.876_877delinsTG	ENSP00000387393.2:p.Ala292=
ENST00000572904.5:c.876_877delinsTG	ENSP00000461484.1:p.Ala292=
ENST00000574590.5:c.876_877delinsTG	ENSP00000461812.1:p.Ala292=
ENST00000575318.5:c.876_877delinsTG	ENSP00000461299.1:p.Ala292=
NM_001193465.1:c.876_877delinsTG	NP_001180394.1:p.Ala292=
NM_001193466.1:c.876_877delinsTG	NP_001180395.1:p.Ala292=
NM_015443.3:c.876_877delinsTG	NP_056258.1:p.Ala292=
XM_006721823.1:c.876_877delinsTG	XP_006721886.1:p.Ala292=
XM_006721824.2:c.876_877delinsTG	XP_006721887.1:p.Ala292=
XM_011524628.1:c.876_877delinsTG	XP_011522930.1:p.Ala292=
XM_011524629.1:c.876_877delinsTG	XP_011522931.1:p.Ala292=
XM_011524630.1:c.876_877delinsTG	XP_011522932.1:p.Ala292=
XM_011524631.1:c.876_877delinsTG	XP_011522933.1:p.Ala292=
XM_006721823.2:c.876_877delinsTG	XP_006721886.1:p.Ala292=
XM_006721824.4:c.876_877delinsTG	XP_006721887.1:p.Ala292=
XM_011524628.3:c.876_877delinsTG	XP_011522930.1:p.Ala292=
XM_011524629.3:c.876_877delinsTG	XP_011522931.1:p.Ala292=
XM_011524630.3:c.876_877delinsTG	XP_011522932.1:p.Ala292=
XM_011524631.3:c.876_877delinsTG	XP_011522933.1:p.Ala292=
XM_017024488.2:c.876_877delinsTG	XP_016879977.1:p.Ala292=
XM_017024489.1:c.876_877delinsTG	XP_016879978.1:p.Ala292=
NM_001193466.2:c.876_877delinsTG	NP_001180395.1:p.Ala292=
NM_015443.4:c.876_877delinsTG MANE Select	NP_056258.1:p.Ala292=
NM_001193465.2:c.876_877delinsTG	NP_001180394.1:p.Ala292=
NM_001379198.1:c.876_877delinsTG	NP_001366127.1:p.Ala292=