Canonical Allele Identifier: CA1538249763
Gene: AMACR HGNC NCBI
C1QTNF3-AMACR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008045G= , CM000667.2:g.34008045G= GRCh38
NC_000005.9:g.34008150G= , CM000667.1:g.34008150G= GRCh37
NC_000005.8:g.34043907G= NCBI36
NG_016211.1:g.5071C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335606.11:c.-26C= (AMACR) MANE Select ENSP00000334424.6:n.-26C=
ENST00000335606.10:c.-26C= (AMACR) ENSP00000334424.6:n.-26C=
ENST00000382079.3:c.690-2146C= (C1QTNF3-AMACR) ENSP00000371511.3:n.690-2146C=
ENST00000426255.6:c.-26C= (AMACR) ENSP00000476965.1:n.-26C=
ENST00000502637.5:c.-26C= (AMACR) ENSP00000424351.1:n.-26C=
NM_001167595.1:c.-26C= (AMACR) NP_001161067.1:n.-26C=
NM_014324.5:c.-26C= (AMACR) NP_055139.4:n.-26C=
NM_203382.2:c.-26C= (AMACR) NP_976316.1:n.-26C=
NR_037951.1:n.765-2146C= (C1QTNF3-AMACR)
NM_014324.6:c.-26C= (AMACR) MANE Select NP_055139.4:n.-26C=
NM_001167595.2:c.-26C= (AMACR) NP_001161067.1:n.-26C=
NM_203382.3:c.-26C= (AMACR) NP_976316.1:n.-26C=