Canonical Allele Identifier: CA1291842307

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137988415_137988416delinsAG , CM000664.2:g.137988415_137988416delinsAG	GRCh38
NC_000002.11:g.138745985_138745986delinsAG , CM000664.1:g.138745985_138745986delinsAG	GRCh37
NC_000002.10:g.138462455_138462456delinsAG	NCBI36
NG_012966.1:g.29178_29179delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.191-12503_191-12502delinsAG MANE Select	ENSP00000280097.3:n.191-12503_191-12502delinsAG
ENST00000280097.4:c.191-12503_191-12502delinsAG	ENSP00000280097.3:n.191-12503_191-12502delinsAG
ENST00000410115.5:c.191-12503_191-12502delinsAG	ENSP00000386940.1:n.191-12503_191-12502delinsAG
ENST00000467390.5:n.203-12503_203-12502delinsAG
ENST00000475675.5:c.*456-3401_*456-3400delinsAG	ENSP00000419415.1:n.*456-3401_*456-3400delinsAG
ENST00000480534.1:n.169-150_169-149delinsAG
ENST00000485653.1:n.123-12503_123-12502delinsAG
NM_006895.2:c.191-12503_191-12502delinsAG	NP_008826.1:n.191-12503_191-12502delinsAG
XM_011511063.1:c.89-12503_89-12502delinsAG	XP_011509365.1:n.89-12503_89-12502delinsAG
XM_011511064.1:c.-188-12503_-188-12502delinsAG	XP_011509366.1:n.-188-12503_-188-12502delinsAG
XM_011511064.2:c.-188-12503_-188-12502delinsAG	XP_011509366.1:n.-188-12503_-188-12502delinsAG
XM_017003948.1:c.89-12503_89-12502delinsAG	XP_016859437.1:n.89-12503_89-12502delinsAG
XM_017003949.2:c.191-12503_191-12502delinsAG	XP_016859438.1:n.191-12503_191-12502delinsAG
XR_001739719.1:n.1040-7737_1040-7736delinsCT
XR_002959286.1:n.578-12503_578-12502delinsAG
NM_006895.3:c.191-12503_191-12502delinsAG MANE Select	NP_008826.1:n.191-12503_191-12502delinsAG