Canonical Allele Identifier: CA1291842246

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137988256_137988257delinsTG , CM000664.2:g.137988256_137988257delinsTG	GRCh38
NC_000002.11:g.138745826_138745827delinsTG , CM000664.1:g.138745826_138745827delinsTG	GRCh37
NC_000002.10:g.138462296_138462297delinsTG	NCBI36
NG_012966.1:g.29019_29020delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.191-12662_191-12661delinsTG MANE Select	ENSP00000280097.3:n.191-12662_191-12661delinsTG
ENST00000280097.4:c.191-12662_191-12661delinsTG	ENSP00000280097.3:n.191-12662_191-12661delinsTG
ENST00000410115.5:c.191-12662_191-12661delinsTG	ENSP00000386940.1:n.191-12662_191-12661delinsTG
ENST00000467390.5:n.203-12662_203-12661delinsTG
ENST00000475675.5:c.*456-3560_*456-3559delinsTG	ENSP00000419415.1:n.*456-3560_*456-3559delinsTG
ENST00000480534.1:n.169-309_169-308delinsTG
ENST00000485653.1:n.123-12662_123-12661delinsTG
NM_006895.2:c.191-12662_191-12661delinsTG	NP_008826.1:n.191-12662_191-12661delinsTG
XM_011511063.1:c.89-12662_89-12661delinsTG	XP_011509365.1:n.89-12662_89-12661delinsTG
XM_011511064.1:c.-188-12662_-188-12661delinsTG	XP_011509366.1:n.-188-12662_-188-12661delinsTG
XM_011511064.2:c.-188-12662_-188-12661delinsTG	XP_011509366.1:n.-188-12662_-188-12661delinsTG
XM_017003948.1:c.89-12662_89-12661delinsTG	XP_016859437.1:n.89-12662_89-12661delinsTG
XM_017003949.2:c.191-12662_191-12661delinsTG	XP_016859438.1:n.191-12662_191-12661delinsTG
XR_001739719.1:n.1040-7578_1040-7577delinsCA
XR_002959286.1:n.578-12662_578-12661delinsTG
NM_006895.3:c.191-12662_191-12661delinsTG MANE Select	NP_008826.1:n.191-12662_191-12661delinsTG