Canonical Allele Identifier: CA12806846
Gene: MSR1 HGNC NCBI

Linked Data

dbSNP Id: rs33959637
gnomAD v2: 8-16012710-G-T
gnomAD v3: 8-16155201-G-T
gnomAD v4: 8-16155201-G-T
MyVariant Identifiers: chr8:g.16012710G>T (hg19) chr8:g.16155201G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16155201G>T , CM000670.2:g.16155201G>T GRCh38
NC_000008.10:g.16012710G>T , CM000670.1:g.16012710G>T GRCh37
NC_000008.9:g.16057081G>T NCBI36
NG_012102.1:g.42591C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262101.10:c.818-57C>A MANE Select ENSP00000262101.5:n.818-57C>A
ENST00000262101.9:c.818-57C>A ENSP00000262101.5:n.818-57C>A
ENST00000350896.3:c.818-57C>A ENSP00000262100.3:n.818-57C>A
ENST00000355282.6:c.818-57C>A ENSP00000347430.2:n.818-57C>A
ENST00000381998.8:c.818-57C>A ENSP00000371428.4:n.818-57C>A
ENST00000445506.6:c.872-57C>A ENSP00000405453.2:n.872-57C>A
ENST00000519060.6:c.*177-57C>A ENSP00000428865.1:n.*177-57C>A
ENST00000522672.5:c.188-57C>A ENSP00000430536.1:n.188-57C>A
NM_002445.3:c.818-57C>A NP_002436.1:n.818-57C>A
NM_138715.2:c.818-57C>A NP_619729.1:n.818-57C>A
NM_138716.2:c.818-57C>A NP_619730.1:n.818-57C>A
NM_001363744.1:c.872-57C>A NP_001350673.1:n.872-57C>A
XM_024447161.1:c.872-57C>A XP_024302929.1:n.872-57C>A
NM_138715.3:c.818-57C>A MANE Select NP_619729.1:n.818-57C>A
NM_002445.4:c.818-57C>A NP_002436.1:n.818-57C>A
NM_138716.3:c.818-57C>A NP_619730.1:n.818-57C>A
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