Canonical Allele Identifier: CA354671579
Gene: MRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138372951G>A , CM000665.2:g.138372951G>A GRCh38
NC_000003.11:g.138091793G>A , CM000665.1:g.138091793G>A GRCh37
NC_000003.10:g.139574483G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423968.7:c.68G>A MANE Select ENSP00000389682.2:p.Gly23Asp
ENST00000289104.8:c.68G>A ENSP00000289104.4:p.Gly23Asp
ENST00000423968.6:c.68G>A ENSP00000389682.2:p.Gly23Asp
ENST00000464896.5:c.-36+23919G>A ENSP00000419582.1:n.-36+23919G>A
ENST00000474559.1:c.68G>A ENSP00000418356.1:p.Gly23Asp
ENST00000475711.5:c.68G>A ENSP00000417092.1:p.Gly23Asp
ENST00000494949.5:c.-36+24184G>A ENSP00000417685.1:n.-36+24184G>A
ENST00000614350.4:c.-35-24373G>A ENSP00000484586.1:n.-35-24373G>A
ENST00000621127.4:c.-36+24184G>A ENSP00000481637.1:n.-36+24184G>A
NM_001085049.2:c.68G>A NP_001078518.1:p.Gly23Asp
NM_001252090.1:c.68G>A NP_001239019.1:p.Gly23Asp
NM_001252091.1:c.-35-24373G>A NP_001239020.1:n.-35-24373G>A
NM_001252092.1:c.-36+23919G>A NP_001239021.1:n.-36+23919G>A
NM_001252093.1:c.-36+24184G>A NP_001239022.1:n.-36+24184G>A
NM_012219.4:c.68G>A NP_036351.3:p.Gly23Asp
XM_005247228.1:c.68G>A XP_005247285.1:p.Gly23Asp
XM_005247229.2:c.68G>A XP_005247286.1:p.Gly23Asp
XM_017005887.2:c.68G>A XP_016861376.1:p.Gly23Asp
XM_024453396.1:c.68G>A XP_024309164.1:p.Gly23Asp
XM_024453397.1:c.68G>A XP_024309165.1:p.Gly23Asp
XM_024453398.1:c.68G>A XP_024309166.1:p.Gly23Asp
NM_001085049.3:c.68G>A MANE Select NP_001078518.1:p.Gly23Asp
NM_001252090.2:c.68G>A NP_001239019.1:p.Gly23Asp
NM_001252092.2:c.-36+23919G>A NP_001239021.1:n.-36+23919G>A
NM_001252093.2:c.-36+24184G>A NP_001239022.1:n.-36+24184G>A