Canonical Allele Identifier: CA2533485863

Gene: MRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138369310T>C , CM000665.2:g.138369310T>C	GRCh38
NC_000003.11:g.138088152T>C , CM000665.1:g.138088152T>C	GRCh37
NC_000003.10:g.139570842T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000423968.7:c.-18-3556T>C MANE Select	ENSP00000389682.2:n.-18-3556T>C
ENST00000289104.8:c.-18-3556T>C	ENSP00000289104.4:n.-18-3556T>C
ENST00000423968.6:c.-18-3556T>C	ENSP00000389682.2:n.-18-3556T>C
ENST00000464896.5:c.-36+20278T>C	ENSP00000419582.1:n.-36+20278T>C
ENST00000474559.1:c.-18-3556T>C	ENSP00000418356.1:n.-18-3556T>C
ENST00000475711.5:c.-18-3556T>C	ENSP00000417092.1:n.-18-3556T>C
ENST00000494949.5:c.-36+20543T>C	ENSP00000417685.1:n.-36+20543T>C
ENST00000614350.4:c.-36+20985T>C	ENSP00000484586.1:n.-36+20985T>C
ENST00000621127.4:c.-36+20543T>C	ENSP00000481637.1:n.-36+20543T>C
NM_001085049.2:c.-18-3556T>C	NP_001078518.1:n.-18-3556T>C
NM_001252090.1:c.-18-3556T>C	NP_001239019.1:n.-18-3556T>C
NM_001252091.1:c.-36+20985T>C	NP_001239020.1:n.-36+20985T>C
NM_001252092.1:c.-36+20278T>C	NP_001239021.1:n.-36+20278T>C
NM_001252093.1:c.-36+20543T>C	NP_001239022.1:n.-36+20543T>C
NM_012219.4:c.-18-3556T>C	NP_036351.3:n.-18-3556T>C
XM_005247228.1:c.-18-3556T>C	XP_005247285.1:n.-18-3556T>C
XM_005247229.2:c.-18-3556T>C	XP_005247286.1:n.-18-3556T>C
XM_017005887.2:c.-18-3556T>C	XP_016861376.1:n.-18-3556T>C
XM_024453396.1:c.-18-3556T>C	XP_024309164.1:n.-18-3556T>C
XM_024453397.1:c.-18-3556T>C	XP_024309165.1:n.-18-3556T>C
XM_024453398.1:c.-18-3556T>C	XP_024309166.1:n.-18-3556T>C
NM_001085049.3:c.-18-3556T>C MANE Select	NP_001078518.1:n.-18-3556T>C
NM_001252090.2:c.-18-3556T>C	NP_001239019.1:n.-18-3556T>C
NM_001252092.2:c.-36+20278T>C	NP_001239021.1:n.-36+20278T>C
NM_001252093.2:c.-36+20543T>C	NP_001239022.1:n.-36+20543T>C