Canonical Allele Identifier: CA647211347

Gene: HNMT

Linked Data

• COSMIC: COSN182104 ; COSN182107

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137988449_137988450insG , CM000664.2:g.137988449_137988450insG	GRCh38
NC_000002.11:g.138746019_138746020insG , CM000664.1:g.138746019_138746020insG	GRCh37
NC_000002.10:g.138462489_138462490insG	NCBI36
NG_012966.1:g.29212_29213insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.191-12469_191-12468insG MANE Select	ENSP00000280097.3:n.191-12469_191-12468insG
ENST00000280097.4:c.191-12469_191-12468insG	ENSP00000280097.3:n.191-12469_191-12468insG
ENST00000410115.5:c.191-12469_191-12468insG	ENSP00000386940.1:n.191-12469_191-12468insG
ENST00000467390.5:n.203-12469_203-12468insG
ENST00000475675.5:c.*456-3367_*456-3366insG	ENSP00000419415.1:n.*456-3367_*456-3366insG
ENST00000480534.1:n.169-116_169-115insG
ENST00000485653.1:n.123-12469_123-12468insG
NM_006895.2:c.191-12469_191-12468insG	NP_008826.1:n.191-12469_191-12468insG
XM_011511063.1:c.89-12469_89-12468insG	XP_011509365.1:n.89-12469_89-12468insG
XM_011511064.1:c.-188-12469_-188-12468insG	XP_011509366.1:n.-188-12469_-188-12468insG
XM_011511064.2:c.-188-12469_-188-12468insG	XP_011509366.1:n.-188-12469_-188-12468insG
XM_017003948.1:c.89-12469_89-12468insG	XP_016859437.1:n.89-12469_89-12468insG
XM_017003949.2:c.191-12469_191-12468insG	XP_016859438.1:n.191-12469_191-12468insG
XR_001739719.1:n.1040-7771_1040-7770insC
XR_002959286.1:n.578-12469_578-12468insG
NM_006895.3:c.191-12469_191-12468insG MANE Select	NP_008826.1:n.191-12469_191-12468insG