Canonical Allele Identifier: CA148628463

Gene: MAP3K5

Linked Data

• dbSNP Id: rs141341865
• gnomAD v2: 6-136899916-C-T
• gnomAD v3: 6-136578778-C-T
• gnomAD v4: 6-136578778-C-T
• MyVariant Identifiers: chr6:g.136899916C>T (hg19) ; chr6:g.136578778C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136578778C>T , CM000668.2:g.136578778C>T	GRCh38
NC_000006.11:g.136899916C>T , CM000668.1:g.136899916C>T	GRCh37
NC_000006.10:g.136941609C>T	NCBI36
NG_011965.1:g.218741G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698928.1:c.3844+1523G>A	ENSP00000514039.1:n.3844+1523G>A
ENST00000359015.5:c.3517+1523G>A MANE Select	ENSP00000351908.4:n.3517+1523G>A
ENST00000359015.4:c.3517+1523G>A	ENSP00000351908.4:n.3517+1523G>A
NM_005923.3:c.3517+1523G>A	NP_005914.1:n.3517+1523G>A
XM_011535837.1:c.3412+1523G>A	XP_011534139.1:n.3412+1523G>A
XM_011535838.1:c.3520+1523G>A	XP_011534140.1:n.3520+1523G>A
XM_011535839.1:c.3520+1523G>A	XP_011534141.1:n.3520+1523G>A
XM_011535839.3:c.3847+1523G>A	XP_011534141.2:n.3847+1523G>A
XM_017010870.1:c.3847+1523G>A	XP_016866359.1:n.3847+1523G>A
XM_017010871.1:c.3844+1523G>A	XP_016866360.1:n.3844+1523G>A
XM_017010872.1:c.3847+1523G>A	XP_016866361.1:n.3847+1523G>A
XM_017010873.1:c.3844+1523G>A	XP_016866362.1:n.3844+1523G>A
XM_017010874.1:c.3739+1523G>A	XP_016866363.1:n.3739+1523G>A
XM_017010875.1:c.3736+1523G>A	XP_016866364.1:n.3736+1523G>A
XM_017010876.1:c.2938+1523G>A	XP_016866365.1:n.2938+1523G>A
XM_017010877.1:c.2938+1523G>A	XP_016866366.1:n.2938+1523G>A
NM_005923.4:c.3517+1523G>A MANE Select	NP_005914.1:n.3517+1523G>A