Canonical Allele Identifier: CA1291842331

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137988469C= , CM000664.2:g.137988469C=	GRCh38
NC_000002.11:g.138746039C= , CM000664.1:g.138746039C=	GRCh37
NC_000002.10:g.138462509C=	NCBI36
NG_012966.1:g.29232C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.191-12449C= MANE Select	ENSP00000280097.3:n.191-12449C=
ENST00000280097.4:c.191-12449C=	ENSP00000280097.3:n.191-12449C=
ENST00000410115.5:c.191-12449C=	ENSP00000386940.1:n.191-12449C=
ENST00000467390.5:n.203-12449C=
ENST00000475675.5:c.*456-3347C=	ENSP00000419415.1:n.*456-3347C=
ENST00000480534.1:n.169-96C=
ENST00000485653.1:n.123-12449C=
NM_006895.2:c.191-12449C=	NP_008826.1:n.191-12449C=
XM_011511063.1:c.89-12449C=	XP_011509365.1:n.89-12449C=
XM_011511064.1:c.-188-12449C=	XP_011509366.1:n.-188-12449C=
XM_011511064.2:c.-188-12449C=	XP_011509366.1:n.-188-12449C=
XM_017003948.1:c.89-12449C=	XP_016859437.1:n.89-12449C=
XM_017003949.2:c.191-12449C=	XP_016859438.1:n.191-12449C=
XR_001739719.1:n.1040-7790G=
XR_002959286.1:n.578-12449C=
NM_006895.3:c.191-12449C= MANE Select	NP_008826.1:n.191-12449C=