Canonical Allele Identifier: CA11379793
Gene: MRAS HGNC NCBI

Linked Data

dbSNP Id: rs2306374

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138401110T>C , CM000665.2:g.138401110T>C GRCh38
NC_000003.11:g.138119952T>C , CM000665.1:g.138119952T>C GRCh37
NC_000003.10:g.139602642T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423968.7:c.527+497T>C MANE Select ENSP00000389682.2:n.527+497T>C
ENST00000289104.8:c.527+497T>C ENSP00000289104.4:n.527+497T>C
ENST00000423968.6:c.527+497T>C ENSP00000389682.2:n.527+497T>C
ENST00000464896.5:c.299+497T>C ENSP00000419582.1:n.299+497T>C
ENST00000474559.1:c.527+497T>C ENSP00000418356.1:n.527+497T>C
ENST00000478647.1:n.405+497T>C
ENST00000494949.5:c.299+497T>C ENSP00000417685.1:n.299+497T>C
ENST00000614350.4:c.299+497T>C ENSP00000484586.1:n.299+497T>C
ENST00000621127.4:c.299+497T>C ENSP00000481637.1:n.299+497T>C
NM_001085049.2:c.527+497T>C NP_001078518.1:n.527+497T>C
NM_001252090.1:c.527+497T>C NP_001239019.1:n.527+497T>C
NM_001252091.1:c.299+497T>C NP_001239020.1:n.299+497T>C
NM_001252092.1:c.299+497T>C NP_001239021.1:n.299+497T>C
NM_001252093.1:c.299+497T>C NP_001239022.1:n.299+497T>C
NM_012219.4:c.527+497T>C NP_036351.3:n.527+497T>C
XM_005247228.1:c.527+497T>C XP_005247285.1:n.527+497T>C
XM_005247229.2:c.*18+497T>C XP_005247286.1:n.*18+497T>C
XM_017005887.2:c.527+497T>C XP_016861376.1:n.527+497T>C
XM_024453396.1:c.527+497T>C XP_024309164.1:n.527+497T>C
XM_024453397.1:c.*18+497T>C XP_024309165.1:n.*18+497T>C
XM_024453398.1:c.*18+497T>C XP_024309166.1:n.*18+497T>C
NM_001085049.3:c.527+497T>C MANE Select NP_001078518.1:n.527+497T>C
NM_001252090.2:c.527+497T>C NP_001239019.1:n.527+497T>C
NM_001252092.2:c.299+497T>C NP_001239021.1:n.299+497T>C
NM_001252093.2:c.299+497T>C NP_001239022.1:n.299+497T>C