Canonical Allele Identifier: CA359381066

Gene: AMACR C1QTNF3-AMACR

Linked Data

• MyVariant Identifiers: chr5:g.33998746C>A (hg19) ; chr5:g.33998641C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33998641C>A , CM000667.2:g.33998641C>A	GRCh38
NC_000005.9:g.33998746C>A , CM000667.1:g.33998746C>A	GRCh37
NC_000005.8:g.34034503C>A	NCBI36
NG_016211.1:g.14475G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335606.11:c.739G>T (AMACR) MANE Select	ENSP00000334424.6:p.Gly247Ter
ENST00000335606.10:c.739G>T (AMACR)	ENSP00000334424.6:p.Gly247Ter
ENST00000382068.3:c.578G>T (AMACR)	ENSP00000477108.1:p.Arg193Met
ENST00000382072.6:c.578G>T (AMACR)	ENSP00000371504.2:p.Arg193Met
ENST00000382079.3:c.*165G>T (C1QTNF3-AMACR)	ENSP00000371511.3:n.*165G>T
ENST00000382085.7:c.739G>T (AMACR)	ENSP00000371517.3:p.Gly247Ter
ENST00000426255.6:c.739G>T (AMACR)	ENSP00000476965.1:p.Gly247Cys
ENST00000502637.5:c.694G>T (AMACR)	ENSP00000424351.1:p.Gly232Ter
ENST00000506639.5:c.578G>T (AMACR)	ENSP00000427227.1:p.Arg193Ile
ENST00000512079.5:c.739G>T (AMACR)	ENSP00000477411.1:p.Gly247Cys
ENST00000514195.1:n.590G>T (AMACR)
NM_001167595.1:c.739G>T (AMACR)	NP_001161067.1:p.Gly247Ter
NM_014324.5:c.739G>T (AMACR)	NP_055139.4:p.Gly247Ter
NM_203382.2:c.578G>T (AMACR)	NP_976316.1:p.Arg193Met
NR_037951.1:n.1095G>T (C1QTNF3-AMACR)
NM_014324.6:c.739G>T (AMACR) MANE Select	NP_055139.4:p.Gly247Ter
NM_001167595.2:c.739G>T (AMACR)	NP_001161067.1:p.Gly247Ter
NM_203382.3:c.578G>T (AMACR)	NP_976316.1:p.Arg193Met