Canonical Allele Identifier: CA1139659736
Community Standard Title: NM_145331.3(MAP3K7):c.737-7A>G
Gene: MAP3K7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.90552186T>C , CM000668.2:g.90552186T>C GRCh38
NC_000006.11:g.91261905T>C , CM000668.1:g.91261905T>C GRCh37
NC_000006.10:g.91318626T>C NCBI36
NG_011966.2:g.40003A>G

Transcript Alleles

HGVS Amino-acid Change
NM_145331.3:c.737-7A>G MANE Select NP_663304.1:n.737-7A>G
ENST00000369329.8:c.737-7A>G MANE Select ENSP00000358335.3:n.737-7A>G
NM_003188.3:c.737-7A>G NP_003179.1:n.737-7A>G
NM_003188.4:c.737-7A>G NP_003179.1:n.737-7A>G
NM_145331.2:c.737-7A>G NP_663304.1:n.737-7A>G
NM_145332.2:c.737-7A>G NP_663305.1:n.737-7A>G
NM_145332.3:c.737-7A>G NP_663305.1:n.737-7A>G
NM_145333.2:c.737-7A>G NP_663306.1:n.737-7A>G
NM_145333.3:c.737-7A>G NP_663306.1:n.737-7A>G
ENST00000369320.1:c.-1720-7A>G ENSP00000358326.1:n.-1720-7A>G
ENST00000369325.7:c.737-7A>G ENSP00000358331.3:n.737-7A>G
ENST00000369327.7:c.737-7A>G ENSP00000358333.3:n.737-7A>G
ENST00000369329.7:c.737-7A>G ENSP00000358335.3:n.737-7A>G
ENST00000369332.7:c.737-7A>G ENSP00000358338.3:n.737-7A>G
ENST00000700580.1:c.737-7A>G ENSP00000515074.1:n.737-7A>G
ENST00000700581.1:c.737-7A>G ENSP00000515075.1:n.737-7A>G
ENST00000700582.1:c.*592-7A>G ENSP00000515076.1:n.*592-7A>G
ENST00000700583.1:c.*343-7A>G ENSP00000515077.1:n.*343-7A>G
ENST00000700584.1:c.*698-7A>G ENSP00000515078.1:n.*698-7A>G
ENST00000700587.1:c.*676-7A>G ENSP00000515080.1:n.*676-7A>G
ENST00000700588.1:n.803-7A>G
ENST00000700589.1:c.*141-7A>G ENSP00000515081.1:n.*141-7A>G
ENST00000700590.1:n.926-7A>G
ENST00000700591.1:c.671-7A>G ENSP00000515082.1:n.671-7A>G
ENST00000700592.1:c.812-7A>G ENSP00000515083.1:n.812-7A>G
ENST00000700593.1:c.428-7A>G ENSP00000515084.1:n.428-7A>G
ENST00000700594.1:c.*491-7A>G ENSP00000515085.1:n.*491-7A>G
ENST00000703100.1:c.*70-7A>G ENSP00000515168.1:n.*70-7A>G
ENST00000703101.1:c.121-28403A>G ENSP00000515169.1:n.121-28403A>G
XM_006715553.2:c.347-7A>G XP_006715616.1:n.347-7A>G
XM_006715553.3:c.347-7A>G XP_006715616.1:n.347-7A>G
XM_017011226.2:c.347-7A>G XP_016866715.1:n.347-7A>G