Canonical Allele Identifier: CA1328678657

Gene: AAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218265791G= , CM000664.2:g.218265791G=	GRCh38
NC_000002.11:g.219130514G= , CM000664.1:g.219130514G=	GRCh37
NC_000002.10:g.218838758G=	NCBI36
NG_017060.1:g.400G=
NG_033036.1:g.9380C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248450.9:c.879+40C= MANE Select	ENSP00000248450.4:n.879+40C=
ENST00000248450.8:c.879+40C=	ENSP00000248450.4:n.879+40C=
ENST00000420660.5:c.822+40C=	ENSP00000416394.1:n.822+40C=
ENST00000422731.1:c.143+40C=
ENST00000444053.5:c.882+40C=	ENSP00000403343.1:n.882+40C=
ENST00000465442.1:n.642C=
ENST00000475678.5:n.1333C=
ENST00000489767.5:n.949C=
ENST00000494720.5:n.131C=
NM_001087.4:c.879+40C=	NP_001078.2:n.879+40C=
NM_001302545.1:c.882+40C=	NP_001289474.1:n.882+40C=
XM_024452712.1:c.879+40C=	XP_024308480.1:n.879+40C=
NM_001087.5:c.879+40C= MANE Select	NP_001078.2:n.879+40C=
NM_001302545.2:c.882+40C=	NP_001289474.1:n.882+40C=