Canonical Allele Identifier: CA11379795

Gene: MRAS

Linked Data

• ClinVar Variation Id: 1650099
• ClinVar RCV Id: RCV002148842
• dbSNP Id: rs9818870
• gnomAD v2: 3-138122122-C-T
• gnomAD v3: 3-138403280-C-T
• gnomAD v4: 3-138403280-C-T
• MyVariant Identifiers: chr3:g.138122122C>T (hg19) ; chr3:g.138403280C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138403280C>T , CM000665.2:g.138403280C>T	GRCh38
NC_000003.11:g.138122122C>T , CM000665.1:g.138122122C>T	GRCh37
NC_000003.10:g.139604812C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000423968.7:c.*1011C>T MANE Select	ENSP00000389682.2:n.*1011C>T
ENST00000289104.8:c.*1011C>T	ENSP00000289104.4:n.*1011C>T
ENST00000614350.4:c.*1011C>T	ENSP00000484586.1:n.*1011C>T
ENST00000621127.4:c.*1011C>T	ENSP00000481637.1:n.*1011C>T
NM_001085049.2:c.*1011C>T	NP_001078518.1:n.*1011C>T
NM_001252090.1:c.*1011C>T	NP_001239019.1:n.*1011C>T
NM_001252091.1:c.*1011C>T	NP_001239020.1:n.*1011C>T
NM_001252092.1:c.*1011C>T	NP_001239021.1:n.*1011C>T
NM_001252093.1:c.*1011C>T	NP_001239022.1:n.*1011C>T
NM_012219.4:c.*1011C>T	NP_036351.3:n.*1011C>T
XM_005247228.1:c.*1011C>T	XP_005247285.1:n.*1011C>T
XM_005247229.2:c.*1129C>T	XP_005247286.1:n.*1129C>T
XM_017005887.2:c.*1011C>T	XP_016861376.1:n.*1011C>T
XM_024453396.1:c.*1011C>T	XP_024309164.1:n.*1011C>T
XM_024453397.1:c.*1129C>T	XP_024309165.1:n.*1129C>T
XM_024453398.1:c.*1129C>T	XP_024309166.1:n.*1129C>T
NM_001085049.3:c.*1011C>T MANE Select	NP_001078518.1:n.*1011C>T
NM_001252090.2:c.*1011C>T	NP_001239019.1:n.*1011C>T
NM_001252092.2:c.*1011C>T	NP_001239021.1:n.*1011C>T
NM_001252093.2:c.*1011C>T	NP_001239022.1:n.*1011C>T