Canonical Allele Identifier: CA8618686
Community Standard Title: NM_015443.4(KANSL1):c.1900G>A (p.Ala634Thr)
Gene: KANSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46050653C>T , CM000679.2:g.46050653C>T GRCh38
NC_000017.10:g.44128019C>T , CM000679.1:g.44128019C>T GRCh37
NC_000017.9:g.41483871C>T NCBI36
NG_032784.1:g.179722G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015443.4:c.1900G>A MANE Select NP_056258.1:p.Ala634Thr
ENST00000432791.7:c.1900G>A MANE Select ENSP00000387393.3:p.Ala634Thr
NM_001193465.1:c.1900G>A NP_001180394.1:p.Ala634Thr
NM_001193465.2:c.1900G>A NP_001180394.1:p.Ala634Thr
NM_001193466.1:c.1900G>A NP_001180395.1:p.Ala634Thr
NM_001193466.2:c.1900G>A NP_001180395.1:p.Ala634Thr
NM_001379198.1:c.1900G>A NP_001366127.1:p.Ala634Thr
NM_015443.3:c.1900G>A NP_056258.1:p.Ala634Thr
ENST00000262419.10:c.1900G>A ENSP00000262419.6:p.Ala634Thr
ENST00000432791.5:c.1900G>A ENSP00000387393.2:p.Ala634Thr
ENST00000571698.2:c.1900G>A ENSP00000459330.2:p.Ala634Thr
ENST00000572904.5:c.1900G>A ENSP00000461484.1:p.Ala634Thr
ENST00000572904.6:c.1900G>A ENSP00000461484.1:p.Ala634Thr
ENST00000574590.5:c.1900G>A ENSP00000461812.1:p.Ala634Thr
ENST00000574590.6:c.1900G>A ENSP00000461812.2:p.Ala634Thr
ENST00000575318.5:c.1900G>A ENSP00000461299.1:p.Ala634Thr
ENST00000575318.6:c.1900G>A ENSP00000461299.1:p.Ala634Thr
ENST00000577114.1:n.697G>A
ENST00000577114.2:n.626G>A
ENST00000638275.1:c.1900G>A ENSP00000492576.1:p.Ala634Thr
ENST00000639150.1:c.634G>A ENSP00000491906.1:p.Ala212Thr
ENST00000639375.1:n.2138G>A
ENST00000639531.1:c.1900G>A ENSP00000491765.1:p.Ala634Thr
ENST00000639853.1:c.1071G>A
ENST00000640636.1:c.42G>A
ENST00000648792.1:c.1900G>A ENSP00000497628.1:p.Ala634Thr
XM_006721823.1:c.1900G>A XP_006721886.1:p.Ala634Thr
XM_006721823.2:c.1900G>A XP_006721886.1:p.Ala634Thr
XM_006721824.2:c.1900G>A XP_006721887.1:p.Ala634Thr
XM_006721824.4:c.1900G>A XP_006721887.1:p.Ala634Thr
XM_011524628.1:c.1900G>A XP_011522930.1:p.Ala634Thr
XM_011524628.3:c.1900G>A XP_011522930.1:p.Ala634Thr
XM_011524629.1:c.1798G>A XP_011522931.1:p.Ala600Thr
XM_011524629.3:c.1798G>A XP_011522931.1:p.Ala600Thr
XM_011524630.1:c.1900G>A XP_011522932.1:p.Ala634Thr
XM_011524630.3:c.1900G>A XP_011522932.1:p.Ala634Thr
XM_011524631.1:c.1900G>A XP_011522933.1:p.Ala634Thr
XM_011524631.3:c.1900G>A XP_011522933.1:p.Ala634Thr
XM_011524632.1:c.670G>A XP_011522934.1:p.Ala224Thr
XM_011524632.3:c.670G>A XP_011522934.1:p.Ala224Thr
XM_017024488.2:c.1900G>A XP_016879977.1:p.Ala634Thr
XM_017024489.1:c.1798G>A XP_016879978.1:p.Ala600Thr