Canonical Allele Identifier: CA1743675460
Gene: MKLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.131336399A= , CM000669.2:g.131336399A= GRCh38
NC_000007.13:g.131021158A= , CM000669.1:g.131021158A= GRCh37
NC_000007.12:g.130671698A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000352689.11:c.98+8402A= MANE Select ENSP00000323527.6:n.98+8402A=
ENST00000352689.10:c.98+8402A= ENSP00000323527.6:n.98+8402A=
ENST00000416992.6:c.-178-39025A= ENSP00000387920.1:n.-178-39025A=
ENST00000421797.6:c.-178-39025A= ENSP00000398094.2:n.-178-39025A=
ENST00000429546.5:c.-178-39025A= ENSP00000399954.1:n.-178-39025A=
ENST00000446815.5:c.-109+8402A= ENSP00000412815.1:n.-109+8402A=
ENST00000458153.5:c.98+8402A= ENSP00000407705.1:n.98+8402A=
ENST00000494286.5:n.142+8402A=
ENST00000494785.5:n.115+8402A=
NM_001145354.1:c.30-39025A= NP_001138826.1:n.30-39025A=
NM_013255.4:c.98+8402A= NP_037387.2:n.98+8402A=
XM_006715993.1:c.98+8402A= XP_006716056.1:n.98+8402A=
XM_011516224.1:c.98+8402A= XP_011514526.1:n.98+8402A=
NM_001321316.1:c.-527+8402A= NP_001308245.1:n.-527+8402A=
XM_006715993.3:c.98+8402A= XP_006716056.1:n.98+8402A=
XM_011516224.3:c.98+8402A= XP_011514526.1:n.98+8402A=
XM_024446766.1:c.-216+8402A= XP_024302534.1:n.-216+8402A=
XM_024446767.1:c.-178-39025A= XP_024302535.1:n.-178-39025A=
NM_013255.5:c.98+8402A= MANE Select NP_037387.2:n.98+8402A=
NM_001145354.2:c.30-39025A= NP_001138826.1:n.30-39025A=
NM_001321316.2:c.-527+8402A= NP_001308245.1:n.-527+8402A=