Canonical Allele Identifier: CA2619464998
Gene: MARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57489881C>T , CM000674.2:g.57489881C>T GRCh38
NC_000012.11:g.57883664C>T , CM000674.1:g.57883664C>T GRCh37
NC_000012.10:g.56169931C>T NCBI36
NG_034077.1:g.6929C>T
NG_023205.2:g.3934G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.415-15C>T MANE Select ENSP00000262027.5:n.415-15C>T
ENST00000262027.9:c.415-15C>T ENSP00000262027.5:n.415-15C>T
ENST00000447721.6:n.133-326C>T
ENST00000537638.6:c.415-15C>T ENSP00000446168.2:n.415-15C>T
ENST00000545888.6:c.414+323C>T ENSP00000439307.2:n.414+323C>T
ENST00000547501.5:c.*51-15C>T ENSP00000447145.1:n.*51-15C>T
ENST00000548674.5:n.384+323C>T
ENST00000549074.5:c.201-326C>T ENSP00000447258.1:n.201-326C>T
ENST00000550449.5:n.528-15C>T
ENST00000551431.5:c.280-326C>T ENSP00000446729.1:n.280-326C>T
ENST00000551892.1:c.110-397C>T ENSP00000450018.1:n.110-397C>T
ENST00000552007.5:c.201-15C>T ENSP00000448576.1:n.201-15C>T
ENST00000552371.1:c.30-15C>T
ENST00000553123.1:n.639-15C>T
ENST00000553162.5:n.438-15C>T
ENST00000628866.2:c.280-326C>T ENSP00000486738.1:n.280-326C>T
ENST00000630571.2:c.201-15C>T ENSP00000485951.1:n.201-15C>T
ENST00000630803.1:c.110-397C>T ENSP00000486356.1:n.110-397C>T
NM_004990.3:c.415-15C>T NP_004981.2:n.415-15C>T
XM_006719398.2:c.-213+323C>T XP_006719461.1:n.-213+323C>T
XM_011538353.1:c.415-15C>T XP_011536655.1:n.415-15C>T
XM_006719398.4:c.-213+323C>T XP_006719461.1:n.-213+323C>T
XR_001748704.2:n.438-15C>T
XR_002957327.1:n.437+323C>T
NM_004990.4:c.415-15C>T MANE Select NP_004981.2:n.415-15C>T