Canonical Allele Identifier: CA412400226

Gene: MAP3K15

Linked Data

• gnomAD v4: X-19362822-T-C
• MyVariant Identifiers: chrX:g.19380940T>C (hg19) ; chrX:g.19362822T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362822T>C , CM000685.2:g.19362822T>C	GRCh38
NC_000023.10:g.19380940T>C , CM000685.1:g.19380940T>C	GRCh37
NC_000023.9:g.19290861T>C	NCBI36
NG_016781.1:g.23930T>C
NG_021184.1:g.157440A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3595A>G MANE Select	ENSP00000345629.4:p.Arg1199Gly
ENST00000338883.8:c.3595A>G	ENSP00000345629.4:p.Arg1199Gly
ENST00000359173.7:c.2923A>G
ENST00000470101.1:n.1013A>G
ENST00000518578.5:n.3657A>G
NM_001001671.3:c.3595A>G	NP_001001671.3:p.Arg1199Gly
XM_011545507.1:c.3250A>G	XP_011543809.1:p.Arg1084Gly
XM_011545508.1:c.3163A>G	XP_011543810.1:p.Arg1055Gly
XM_011545509.1:c.2560A>G	XP_011543811.1:p.Arg854Gly
XM_011545510.1:c.2269A>G	XP_011543812.1:p.Arg757Gly
XM_011545511.1:c.1900A>G	XP_011543813.1:p.Arg634Gly
XM_011545507.3:c.3250A>G	XP_011543809.3:p.Arg1084Gly
XM_011545508.3:c.3163A>G	XP_011543810.3:p.Arg1055Gly
XM_011545510.2:c.2269A>G	XP_011543812.1:p.Arg757Gly
XM_011545511.2:c.1900A>G	XP_011543813.1:p.Arg634Gly
NM_001001671.4:c.3595A>G MANE Select	NP_001001671.3:p.Arg1199Gly