Canonical Allele Identifier: CA1538249767

Gene: AMACR C1QTNF3-AMACR

Linked Data

• dbSNP Id: rs1754058145

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34008049C>G , CM000667.2:g.34008049C>G	GRCh38
NC_000005.9:g.34008154C>G , CM000667.1:g.34008154C>G	GRCh37
NC_000005.8:g.34043911C>G	NCBI36
NG_016211.1:g.5067G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335606.11:c.-30G>C (AMACR) MANE Select	ENSP00000334424.6:n.-30G>C
ENST00000335606.10:c.-30G>C (AMACR)	ENSP00000334424.6:n.-30G>C
ENST00000382079.3:c.690-2150G>C (C1QTNF3-AMACR)	ENSP00000371511.3:n.690-2150G>C
ENST00000426255.6:c.-30G>C (AMACR)	ENSP00000476965.1:n.-30G>C
ENST00000502637.5:c.-30G>C (AMACR)	ENSP00000424351.1:n.-30G>C
NM_001167595.1:c.-30G>C (AMACR)	NP_001161067.1:n.-30G>C
NM_014324.5:c.-30G>C (AMACR)	NP_055139.4:n.-30G>C
NM_203382.2:c.-30G>C (AMACR)	NP_976316.1:n.-30G>C
NR_037951.1:n.765-2150G>C (C1QTNF3-AMACR)
NM_014324.6:c.-30G>C (AMACR) MANE Select	NP_055139.4:n.-30G>C
NM_001167595.2:c.-30G>C (AMACR)	NP_001161067.1:n.-30G>C
NM_203382.3:c.-30G>C (AMACR)	NP_976316.1:n.-30G>C