Canonical Allele Identifier: CA899569814

Gene: MRAS

Linked Data

• ClinVar Variation Id: 2819695
• ClinVar RCV Id: RCV003706410
• dbSNP Id: rs1349118454
• gnomAD v3: 3-138373001-CCTGA-C
• gnomAD v4: 3-138373001-CCTGA-C
• MyVariant Identifiers: chr3:g.138091844_138091847del (hg19) ; chr3:g.138373002_138373005del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138373004_138373007del , CM000665.2:g.138373004_138373007del	GRCh38
NC_000003.11:g.138091846_138091849del , CM000665.1:g.138091846_138091849del	GRCh37
NC_000003.10:g.139574536_139574539del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423968.7:c.121_124del MANE Select	ENSP00000389682.2:p.Asp41MetfsTer10
ENST00000289104.8:c.121_124del	ENSP00000289104.4:p.Asp41MetfsTer10
ENST00000423968.6:c.121_124del	ENSP00000389682.2:p.Asp41MetfsTer10
ENST00000464896.5:c.-36+23972_-36+23975del	ENSP00000419582.1:n.-36+23972_-36+23975del
ENST00000474559.1:c.121_124del	ENSP00000418356.1:p.Asp41MetfsTer10
ENST00000494949.5:c.-36+24237_-36+24240del	ENSP00000417685.1:n.-36+24237_-36+24240del
ENST00000614350.4:c.-35-24320_-35-24317del	ENSP00000484586.1:n.-35-24320_-35-24317del
ENST00000621127.4:c.-36+24237_-36+24240del	ENSP00000481637.1:n.-36+24237_-36+24240del
NM_001085049.2:c.121_124del	NP_001078518.1:p.Asp41MetfsTer10
NM_001252090.1:c.121_124del	NP_001239019.1:p.Asp41MetfsTer10
NM_001252091.1:c.-35-24320_-35-24317del	NP_001239020.1:n.-35-24320_-35-24317del
NM_001252092.1:c.-36+23972_-36+23975del	NP_001239021.1:n.-36+23972_-36+23975del
NM_001252093.1:c.-36+24237_-36+24240del	NP_001239022.1:n.-36+24237_-36+24240del
NM_012219.4:c.121_124del	NP_036351.3:p.Asp41MetfsTer10
XM_005247228.1:c.121_124del	XP_005247285.1:p.Asp41MetfsTer10
XM_005247229.2:c.121_124del	XP_005247286.1:p.Asp41MetfsTer10
XM_017005887.2:c.121_124del	XP_016861376.1:p.Asp41MetfsTer10
XM_024453396.1:c.121_124del	XP_024309164.1:p.Asp41MetfsTer10
XM_024453397.1:c.121_124del	XP_024309165.1:p.Asp41MetfsTer10
XM_024453398.1:c.121_124del	XP_024309166.1:p.Asp41MetfsTer10
NM_001085049.3:c.121_124del MANE Select	NP_001078518.1:p.Asp41MetfsTer10
NM_001252090.2:c.121_124del	NP_001239019.1:p.Asp41MetfsTer10
NM_001252092.2:c.-36+23972_-36+23975del	NP_001239021.1:n.-36+23972_-36+23975del
NM_001252093.2:c.-36+24237_-36+24240del	NP_001239022.1:n.-36+24237_-36+24240del