Canonical Allele Identifier: CA14569665

Gene: FAM210A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.13708575A>G , CM000680.2:g.13708575A>G	GRCh38
NC_000018.9:g.13708574A>G , CM000680.1:g.13708574A>G	GRCh37
NC_000018.8:g.13698574A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651643.1:c.-29+17754T>C MANE Select	ENSP00000498370.1:n.-29+17754T>C
ENST00000322247.7:c.-156-10901T>C	ENSP00000323635.3:n.-156-10901T>C
ENST00000402563.5:c.-29+17754T>C	ENSP00000386115.1:n.-29+17754T>C
ENST00000585785.1:n.264+17754T>C
ENST00000588475.1:n.177+17754T>C
ENST00000591269.1:c.-169+17754T>C	ENSP00000468361.1:n.-169+17754T>C
ENST00000592976.5:c.-29+17754T>C	ENSP00000465396.1:n.-29+17754T>C
NM_001098801.1:c.-169+17754T>C	NP_001092271.1:n.-169+17754T>C
NM_152352.3:c.-29+17754T>C	NP_689565.2:n.-29+17754T>C
XM_006722298.2:c.-29+16710T>C	XP_006722361.1:n.-29+16710T>C
XM_024451083.1:c.-29+16710T>C	XP_024306851.1:n.-29+16710T>C
NM_152352.4:c.-29+17754T>C MANE Select	NP_689565.2:n.-29+17754T>C
NM_001098801.2:c.-169+17754T>C	NP_001092271.1:n.-169+17754T>C