Canonical Allele Identifier: CA2697556877

Gene: MRAS

Linked Data

• ClinVar Variation Id: 2694483
• ClinVar RCV Id: RCV003544159

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138373043dup , CM000665.2:g.138373043dup	GRCh38
NC_000003.11:g.138091885dup , CM000665.1:g.138091885dup	GRCh37
NC_000003.10:g.139574575dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423968.7:c.160dup MANE Select	ENSP00000389682.2:p.Thr54AsnfsTer4
ENST00000289104.8:c.160dup	ENSP00000289104.4:p.Thr54AsnfsTer4
ENST00000423968.6:c.160dup	ENSP00000389682.2:p.Thr54AsnfsTer4
ENST00000464896.5:c.-36+24011dup	ENSP00000419582.1:n.-36+24011dup
ENST00000474559.1:c.160dup	ENSP00000418356.1:p.Thr54AsnfsTer4
ENST00000494949.5:c.-36+24276dup	ENSP00000417685.1:n.-36+24276dup
ENST00000614350.4:c.-35-24281dup	ENSP00000484586.1:n.-35-24281dup
ENST00000621127.4:c.-36+24276dup	ENSP00000481637.1:n.-36+24276dup
NM_001085049.2:c.160dup	NP_001078518.1:p.Thr54AsnfsTer4
NM_001252090.1:c.160dup	NP_001239019.1:p.Thr54AsnfsTer4
NM_001252091.1:c.-35-24281dup	NP_001239020.1:n.-35-24281dup
NM_001252092.1:c.-36+24011dup	NP_001239021.1:n.-36+24011dup
NM_001252093.1:c.-36+24276dup	NP_001239022.1:n.-36+24276dup
NM_012219.4:c.160dup	NP_036351.3:p.Thr54AsnfsTer4
XM_005247228.1:c.160dup	XP_005247285.1:p.Thr54AsnfsTer4
XM_005247229.2:c.160dup	XP_005247286.1:p.Thr54AsnfsTer4
XM_017005887.2:c.160dup	XP_016861376.1:p.Thr54AsnfsTer4
XM_024453396.1:c.160dup	XP_024309164.1:p.Thr54AsnfsTer4
XM_024453397.1:c.160dup	XP_024309165.1:p.Thr54AsnfsTer4
XM_024453398.1:c.160dup	XP_024309166.1:p.Thr54AsnfsTer4
NM_001085049.3:c.160dup MANE Select	NP_001078518.1:p.Thr54AsnfsTer4
NM_001252090.2:c.160dup	NP_001239019.1:p.Thr54AsnfsTer4
NM_001252092.2:c.-36+24011dup	NP_001239021.1:n.-36+24011dup
NM_001252093.2:c.-36+24276dup	NP_001239022.1:n.-36+24276dup