Canonical Allele Identifier: CA12306214
Gene: MAP3K5 HGNC NCBI

Linked Data

dbSNP Id: rs1570056

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136738789T>C , CM000668.2:g.136738789T>C GRCh38
NC_000006.11:g.137059927T>C , CM000668.1:g.137059927T>C GRCh37
NC_000006.10:g.137101620T>C NCBI36
NG_011965.1:g.58730A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698928.1:c.776-18200A>G ENSP00000514039.1:n.776-18200A>G
ENST00000359015.5:c.449-18200A>G MANE Select ENSP00000351908.4:n.449-18200A>G
ENST00000359015.4:c.449-18200A>G ENSP00000351908.4:n.449-18200A>G
NM_005923.3:c.449-18200A>G NP_005914.1:n.449-18200A>G
XM_011535837.1:c.449-18200A>G XP_011534139.1:n.449-18200A>G
XM_011535838.1:c.449-18200A>G XP_011534140.1:n.449-18200A>G
XM_011535839.1:c.449-18200A>G XP_011534141.1:n.449-18200A>G
XM_011535839.3:c.776-18200A>G XP_011534141.2:n.776-18200A>G
XM_017010870.1:c.776-18200A>G XP_016866359.1:n.776-18200A>G
XM_017010871.1:c.776-18200A>G XP_016866360.1:n.776-18200A>G
XM_017010872.1:c.776-18200A>G XP_016866361.1:n.776-18200A>G
XM_017010873.1:c.776-18200A>G XP_016866362.1:n.776-18200A>G
XM_017010874.1:c.776-18200A>G XP_016866363.1:n.776-18200A>G
XM_017010875.1:c.776-18200A>G XP_016866364.1:n.776-18200A>G
XM_017010876.1:c.7-33656A>G XP_016866365.1:n.7-33656A>G
XM_017010877.1:c.7-33656A>G XP_016866366.1:n.7-33656A>G
NM_005923.4:c.449-18200A>G MANE Select NP_005914.1:n.449-18200A>G