Canonical Allele Identifier: CA1291834175

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137970206G= , CM000664.2:g.137970206G=	GRCh38
NC_000002.11:g.138727776G= , CM000664.1:g.138727776G=	GRCh37
NC_000002.10:g.138444246G=	NCBI36
NG_012966.1:g.10969G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.179G= MANE Select	ENSP00000280097.3:p.Gly60=
ENST00000280097.4:c.179G=	ENSP00000280097.3:p.Gly60=
ENST00000329366.8:c.179G=	ENSP00000333259.4:p.Gly60=
ENST00000410115.5:c.179G=	ENSP00000386940.1:p.Gly60=
ENST00000467390.5:n.191G=
ENST00000475675.5:c.*444G=	ENSP00000419415.1:n.*444G=
ENST00000480534.1:n.157G=
ENST00000485653.1:n.122+5578G=
NM_001024075.1:c.179G=	NP_001019246.1:p.Gly60=
NM_006895.2:c.179G=	NP_008826.1:p.Gly60=
XM_011511063.1:c.77G=	XP_011509365.1:p.Gly26=
XM_011511064.1:c.-189+5578G=	XP_011509366.1:n.-189+5578G=
XM_011511064.2:c.-189+5578G=	XP_011509366.1:n.-189+5578G=
XM_017003948.1:c.77G=	XP_016859437.1:p.Gly26=
XM_017003949.2:c.179G=	XP_016859438.1:p.Gly60=
XR_002959286.1:n.566G=
NM_006895.3:c.179G= MANE Select	NP_008826.1:p.Gly60=
NM_001024075.2:c.179G=	NP_001019246.1:p.Gly60=
NM_001024075.3:c.179G=	NP_001019246.1:p.Gly60=