Canonical Allele Identifier: CA11575093
Gene: MRAS HGNC NCBI

Linked Data

dbSNP Id: rs1678443
gnomAD v2: 3-138097534-C-A
gnomAD v3: 3-138378692-C-A
gnomAD v4: 3-138378692-C-A
MyVariant Identifiers: chr3:g.138097534C>A (hg19) chr3:g.138378692C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138378692C>A , CM000665.2:g.138378692C>A GRCh38
NC_000003.11:g.138097534C>A , CM000665.1:g.138097534C>A GRCh37
NC_000003.10:g.139580224C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423968.7:c.193+5616C>A MANE Select ENSP00000389682.2:n.193+5616C>A
ENST00000289104.8:c.193+5616C>A ENSP00000289104.4:n.193+5616C>A
ENST00000423968.6:c.193+5616C>A ENSP00000389682.2:n.193+5616C>A
ENST00000464896.5:c.-35-18632C>A ENSP00000419582.1:n.-35-18632C>A
ENST00000474559.1:c.193+5616C>A ENSP00000418356.1:n.193+5616C>A
ENST00000494949.5:c.-35-18632C>A ENSP00000417685.1:n.-35-18632C>A
ENST00000614350.4:c.-35-18632C>A ENSP00000484586.1:n.-35-18632C>A
ENST00000621127.4:c.-35-18632C>A ENSP00000481637.1:n.-35-18632C>A
NM_001085049.2:c.193+5616C>A NP_001078518.1:n.193+5616C>A
NM_001252090.1:c.193+5616C>A NP_001239019.1:n.193+5616C>A
NM_001252091.1:c.-35-18632C>A NP_001239020.1:n.-35-18632C>A
NM_001252092.1:c.-35-18632C>A NP_001239021.1:n.-35-18632C>A
NM_001252093.1:c.-35-18632C>A NP_001239022.1:n.-35-18632C>A
NM_012219.4:c.193+5616C>A NP_036351.3:n.193+5616C>A
XM_005247228.1:c.193+5616C>A XP_005247285.1:n.193+5616C>A
XM_005247229.2:c.193+5616C>A XP_005247286.1:n.193+5616C>A
XM_017005887.2:c.193+5616C>A XP_016861376.1:n.193+5616C>A
XM_024453396.1:c.193+5616C>A XP_024309164.1:n.193+5616C>A
XM_024453397.1:c.193+5616C>A XP_024309165.1:n.193+5616C>A
XM_024453398.1:c.193+5616C>A XP_024309166.1:n.193+5616C>A
NM_001085049.3:c.193+5616C>A MANE Select NP_001078518.1:n.193+5616C>A
NM_001252090.2:c.193+5616C>A NP_001239019.1:n.193+5616C>A
NM_001252092.2:c.-35-18632C>A NP_001239021.1:n.-35-18632C>A
NM_001252093.2:c.-35-18632C>A NP_001239022.1:n.-35-18632C>A
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