Canonical Allele Identifier: CA354676663

Gene: MRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138400550C>A , CM000665.2:g.138400550C>A	GRCh38
NC_000003.11:g.138119392C>A , CM000665.1:g.138119392C>A	GRCh37
NC_000003.10:g.139602082C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001085049.3:c.464C>A MANE Select	NP_001078518.1:p.Thr155Asn
ENST00000423968.7:c.464C>A MANE Select	ENSP00000389682.2:p.Thr155Asn
NM_001085049.2:c.464C>A	NP_001078518.1:p.Thr155Asn
NM_001252090.1:c.464C>A	NP_001239019.1:p.Thr155Asn
NM_001252090.2:c.464C>A	NP_001239019.1:p.Thr155Asn
NM_001252091.1:c.236C>A	NP_001239020.1:p.Thr79Asn
NM_001252092.1:c.236C>A	NP_001239021.1:p.Thr79Asn
NM_001252092.2:c.236C>A	NP_001239021.1:p.Thr79Asn
NM_001252093.1:c.236C>A	NP_001239022.1:p.Thr79Asn
NM_001252093.2:c.236C>A	NP_001239022.1:p.Thr79Asn
NM_012219.4:c.464C>A	NP_036351.3:p.Thr155Asn
ENST00000289104.8:c.464C>A	ENSP00000289104.4:p.Thr155Asn
ENST00000423968.6:c.464C>A	ENSP00000389682.2:p.Thr155Asn
ENST00000464896.5:c.236C>A	ENSP00000419582.1:p.Thr79Asn
ENST00000474559.1:c.464C>A	ENSP00000418356.1:p.Thr155Asn
ENST00000478647.1:n.342C>A
ENST00000494949.5:c.236C>A	ENSP00000417685.1:p.Thr79Asn
ENST00000614350.4:c.236C>A	ENSP00000484586.1:p.Thr79Asn
ENST00000621127.4:c.236C>A	ENSP00000481637.1:p.Thr79Asn
XM_005247228.1:c.464C>A	XP_005247285.1:p.Thr155Asn
XM_005247229.2:c.468C>A	XP_005247286.1:p.Asn156Lys
XM_017005887.2:c.464C>A	XP_016861376.1:p.Thr155Asn
XM_024453396.1:c.464C>A	XP_024309164.1:p.Thr155Asn
XM_024453397.1:c.468C>A	XP_024309165.1:p.Asn156Lys
XM_024453398.1:c.468C>A	XP_024309166.1:p.Asn156Lys