Canonical Allele Identifier: CA354672403

Gene: MRAS

Linked Data

• ClinVar Variation Id: 635782
• ClinVar RCV Id: RCV000787304 ; RCV002536888
• dbSNP Id: rs1576387876
• MyVariant Identifiers: chr3:g.138116175C>T (hg19) ; chr3:g.138397333C>T (hg38)
• ERepo: CA354672403/MONDO:0021060/087

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138397333C>T , CM000665.2:g.138397333C>T	GRCh38
NC_000003.11:g.138116175C>T , CM000665.1:g.138116175C>T	GRCh37
NC_000003.10:g.139598865C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423968.7:c.203C>T MANE Select	ENSP00000389682.2:p.Thr68Ile
ENST00000289104.8:c.203C>T	ENSP00000289104.4:p.Thr68Ile
ENST00000423968.6:c.203C>T	ENSP00000389682.2:p.Thr68Ile
ENST00000464896.5:c.-26C>T	ENSP00000419582.1:n.-26C>T
ENST00000474559.1:c.203C>T	ENSP00000418356.1:p.Thr68Ile
ENST00000494949.5:c.-26C>T	ENSP00000417685.1:n.-26C>T
ENST00000614350.4:c.-26C>T	ENSP00000484586.1:n.-26C>T
ENST00000621127.4:c.-26C>T	ENSP00000481637.1:n.-26C>T
NM_001085049.2:c.203C>T	NP_001078518.1:p.Thr68Ile
NM_001252090.1:c.203C>T	NP_001239019.1:p.Thr68Ile
NM_001252091.1:c.-26C>T	NP_001239020.1:n.-26C>T
NM_001252092.1:c.-26C>T	NP_001239021.1:n.-26C>T
NM_001252093.1:c.-26C>T	NP_001239022.1:n.-26C>T
NM_012219.4:c.203C>T	NP_036351.3:p.Thr68Ile
XM_005247228.1:c.203C>T	XP_005247285.1:p.Thr68Ile
XM_005247229.2:c.203C>T	XP_005247286.1:p.Thr68Ile
XM_017005887.2:c.203C>T	XP_016861376.1:p.Thr68Ile
XM_024453396.1:c.203C>T	XP_024309164.1:p.Thr68Ile
XM_024453397.1:c.203C>T	XP_024309165.1:p.Thr68Ile
XM_024453398.1:c.203C>T	XP_024309166.1:p.Thr68Ile
NM_001085049.3:c.203C>T MANE Select	NP_001078518.1:p.Thr68Ile
NM_001252090.2:c.203C>T	NP_001239019.1:p.Thr68Ile
NM_001252092.2:c.-26C>T	NP_001239021.1:n.-26C>T
NM_001252093.2:c.-26C>T	NP_001239022.1:n.-26C>T