Canonical Allele Identifier: CA2038898457
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511931A= , CM000674.2:g.57511931A= GRCh38
NC_000012.11:g.57905714A= , CM000674.1:g.57905714A= GRCh37
NC_000012.10:g.56191981A= NCBI36
NG_034077.1:g.28979A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1539+63A= MANE Select ENSP00000262027.5:n.1539+63A=
ENST00000262027.9:c.1539+63A= ENSP00000262027.5:n.1539+63A=
ENST00000447721.6:n.1181+63A=
ENST00000537638.6:c.1539+63A= ENSP00000446168.2:n.1539+63A=
ENST00000545888.6:c.*1040+63A= ENSP00000439307.2:n.*1040+63A=
ENST00000546971.5:n.283+63A=
ENST00000548630.1:n.100+63A=
ENST00000548944.1:c.134-4564A= ENSP00000449071.1:n.134-4564A=
ENST00000549048.1:n.72+63A=
ENST00000628866.2:c.*1040+63A= ENSP00000486738.1:n.*1040+63A=
NM_004990.3:c.1539+63A= NP_004981.2:n.1539+63A=
XM_006719398.2:c.837+63A= XP_006719461.1:n.837+63A=
XM_011538353.1:c.1539+63A= XP_011536655.1:n.1539+63A=
XM_006719398.4:c.837+63A= XP_006719461.1:n.837+63A=
XR_001748704.2:n.1562+63A=
XR_002957327.1:n.1486+63A=
NM_004990.4:c.1539+63A= MANE Select NP_004981.2:n.1539+63A=