Canonical Allele Identifier: CA1838357457
Community Standard Title: NM_004529.4(MLLT3):c.194-18392A=
Gene: MLLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20475178T= , CM000671.2:g.20475178T= GRCh38
NC_000009.11:g.20475176T= , CM000671.1:g.20475176T= GRCh37
NC_000009.10:g.20465176T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_004529.4:c.194-18392A= MANE Select NP_004520.2:n.194-18392A=
ENST00000380338.9:c.194-18392A= MANE Select ENSP00000369695.4:n.194-18392A=
NM_001286691.1:c.185-18392A= NP_001273620.1:n.185-18392A=
NM_001286691.2:c.185-18392A= NP_001273620.1:n.185-18392A=
NM_004529.3:c.194-18392A= NP_004520.2:n.194-18392A=
ENST00000380338.8:c.194-18392A= ENSP00000369695.4:n.194-18392A=
ENST00000475957.1:n.378-60753A=
ENST00000629733.2:c.-1025-18392A= ENSP00000486193.1:n.-1025-18392A=
ENST00000630269.2:c.185-18392A= ENSP00000485996.1:n.185-18392A=
XM_017014726.2:c.194-18392A= XP_016870215.1:n.194-18392A=
XM_017014727.1:c.185-18392A= XP_016870216.1:n.185-18392A=