Canonical Allele Identifier: CA2765835914

Gene: AMACR C1QTNF3-AMACR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34008047A>C , CM000667.2:g.34008047A>C	GRCh38
NC_000005.9:g.34008152A>C , CM000667.1:g.34008152A>C	GRCh37
NC_000005.8:g.34043909A>C	NCBI36
NG_016211.1:g.5069T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335606.11:c.-28T>G (AMACR) MANE Select	ENSP00000334424.6:n.-28T>G
ENST00000335606.10:c.-28T>G (AMACR)	ENSP00000334424.6:n.-28T>G
ENST00000382079.3:c.690-2148T>G (C1QTNF3-AMACR)	ENSP00000371511.3:n.690-2148T>G
ENST00000426255.6:c.-28T>G (AMACR)	ENSP00000476965.1:n.-28T>G
ENST00000502637.5:c.-28T>G (AMACR)	ENSP00000424351.1:n.-28T>G
NM_001167595.1:c.-28T>G (AMACR)	NP_001161067.1:n.-28T>G
NM_014324.5:c.-28T>G (AMACR)	NP_055139.4:n.-28T>G
NM_203382.2:c.-28T>G (AMACR)	NP_976316.1:n.-28T>G
NR_037951.1:n.765-2148T>G (C1QTNF3-AMACR)
NM_014324.6:c.-28T>G (AMACR) MANE Select	NP_055139.4:n.-28T>G
NM_001167595.2:c.-28T>G (AMACR)	NP_001161067.1:n.-28T>G
NM_203382.3:c.-28T>G (AMACR)	NP_976316.1:n.-28T>G