Canonical Allele Identifier: CA1291848208
Gene: HNMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.138001907A= , CM000664.2:g.138001907A= GRCh38
NC_000002.11:g.138759477A= , CM000664.1:g.138759477A= GRCh37
NC_000002.10:g.138475947A= NCBI36
NG_012966.1:g.42670A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000280097.5:c.299-157A= MANE Select ENSP00000280097.3:n.299-157A=
ENST00000280097.4:c.299-157A= ENSP00000280097.3:n.299-157A=
ENST00000410115.5:c.299-157A= ENSP00000386940.1:n.299-157A=
ENST00000467390.5:n.311-157A=
ENST00000485653.1:n.231-157A=
NM_006895.2:c.299-157A= NP_008826.1:n.299-157A=
XM_011511063.1:c.197-157A= XP_011509365.1:n.197-157A=
XM_011511064.1:c.-80-157A= XP_011509366.1:n.-80-157A=
XM_011511064.2:c.-80-157A= XP_011509366.1:n.-80-157A=
XM_017003948.1:c.197-157A= XP_016859437.1:n.197-157A=
XM_017003949.2:c.299-157A= XP_016859438.1:n.299-157A=
XR_001739719.1:n.1039+5082T=
XR_002959286.1:n.686-157A=
NM_006895.3:c.299-157A= MANE Select NP_008826.1:n.299-157A=