Canonical Allele Identifier: CA2575202421
Gene: MARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57489871T>C , CM000674.2:g.57489871T>C GRCh38
NC_000012.11:g.57883654T>C , CM000674.1:g.57883654T>C GRCh37
NC_000012.10:g.56169921T>C NCBI36
NG_034077.1:g.6919T>C
NG_023205.2:g.3944A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.415-25T>C MANE Select ENSP00000262027.5:n.415-25T>C
ENST00000262027.9:c.415-25T>C ENSP00000262027.5:n.415-25T>C
ENST00000447721.6:n.133-336T>C
ENST00000537638.6:c.415-25T>C ENSP00000446168.2:n.415-25T>C
ENST00000545888.6:c.414+313T>C ENSP00000439307.2:n.414+313T>C
ENST00000547501.5:c.*51-25T>C ENSP00000447145.1:n.*51-25T>C
ENST00000548674.5:n.384+313T>C
ENST00000549074.5:c.201-336T>C ENSP00000447258.1:n.201-336T>C
ENST00000550449.5:n.528-25T>C
ENST00000551431.5:c.280-336T>C ENSP00000446729.1:n.280-336T>C
ENST00000551892.1:c.110-407T>C ENSP00000450018.1:n.110-407T>C
ENST00000552007.5:c.201-25T>C ENSP00000448576.1:n.201-25T>C
ENST00000552371.1:c.30-25T>C
ENST00000553123.1:n.639-25T>C
ENST00000553162.5:n.438-25T>C
ENST00000628866.2:c.280-336T>C ENSP00000486738.1:n.280-336T>C
ENST00000630571.2:c.201-25T>C ENSP00000485951.1:n.201-25T>C
ENST00000630803.1:c.110-407T>C ENSP00000486356.1:n.110-407T>C
NM_004990.3:c.415-25T>C NP_004981.2:n.415-25T>C
XM_006719398.2:c.-213+313T>C XP_006719461.1:n.-213+313T>C
XM_011538353.1:c.415-25T>C XP_011536655.1:n.415-25T>C
XM_006719398.4:c.-213+313T>C XP_006719461.1:n.-213+313T>C
XR_001748704.2:n.438-25T>C
XR_002957327.1:n.437+313T>C
NM_004990.4:c.415-25T>C MANE Select NP_004981.2:n.415-25T>C