Canonical Allele Identifier: CA1222560516

Gene: MTARC1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220800221C>G , CM000663.2:g.220800221C>G	GRCh38
NC_000001.10:g.220973563C>G , CM000663.1:g.220973563C>G	GRCh37
NC_000001.9:g.219040186C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000694918.1:c.447+2207C>G	ENSP00000511593.1:n.447+2207C>G
ENST00000694919.1:c.754-640C>G	ENSP00000511594.1:n.754-640C>G
ENST00000694922.1:c.447+2207C>G	ENSP00000511595.1:n.447+2207C>G
ENST00000694923.1:n.866+1946C>G
ENST00000694924.1:n.717+2207C>G
ENST00000366910.10:c.753+2207C>G MANE Select	ENSP00000355877.5:n.753+2207C>G
ENST00000651706.1:c.708+2207C>G	ENSP00000499157.1:n.708+2207C>G
ENST00000366910.9:c.753+2207C>G	ENSP00000355877.5:n.753+2207C>G
ENST00000407981.6:c.529+2156C>G
ENST00000443880.1:c.192+2207C>G	ENSP00000409634.1:n.192+2207C>G
ENST00000472269.1:n.304+2156C>G
ENST00000496110.1:n.1471+2207C>G
NM_022746.3:c.753+2207C>G	NP_073583.3:n.753+2207C>G
XM_011509900.1:c.804+2156C>G	XP_011508202.1:n.804+2156C>G
XM_011509901.1:c.804+2156C>G	XP_011508203.1:n.804+2156C>G
XM_011509903.1:c.555+2156C>G	XP_011508205.1:n.555+2156C>G
XM_011509904.1:c.498+2156C>G	XP_011508206.1:n.498+2156C>G
XM_011509900.3:c.804+2156C>G	XP_011508202.1:n.804+2156C>G
XM_011509903.3:c.555+2156C>G	XP_011508205.1:n.555+2156C>G
XM_011509904.3:c.498+2156C>G	XP_011508206.1:n.498+2156C>G
XM_017002096.2:c.504+2207C>G	XP_016857585.1:n.504+2207C>G
XM_017002097.2:c.447+2207C>G	XP_016857586.1:n.447+2207C>G
XR_001737362.1:n.1176+1946C>G
XR_002957377.1:n.756+1946C>G
NM_022746.4:c.753+2207C>G MANE Select	NP_073583.3:n.753+2207C>G