Canonical Allele Identifier: CA2418227181

Gene: MAP3K15

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362907A= , CM000685.2:g.19362907A=	GRCh38
NC_000023.10:g.19381025A= , CM000685.1:g.19381025A=	GRCh37
NC_000023.9:g.19290946A=	NCBI36
NG_016781.1:g.24015A=
NG_021184.1:g.157355T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3567-57T= MANE Select	ENSP00000345629.4:n.3567-57T=
ENST00000338883.8:c.3567-57T=	ENSP00000345629.4:n.3567-57T=
ENST00000359173.7:c.2895-57T=
ENST00000470101.1:n.985-57T=
ENST00000518578.5:n.3629-57T=
NM_001001671.3:c.3567-57T=	NP_001001671.3:n.3567-57T=
XM_011545507.1:c.3222-57T=	XP_011543809.1:n.3222-57T=
XM_011545508.1:c.3135-57T=	XP_011543810.1:n.3135-57T=
XM_011545509.1:c.2532-57T=	XP_011543811.1:n.2532-57T=
XM_011545510.1:c.2241-57T=	XP_011543812.1:n.2241-57T=
XM_011545511.1:c.1872-57T=	XP_011543813.1:n.1872-57T=
XM_011545507.3:c.3222-57T=	XP_011543809.3:n.3222-57T=
XM_011545508.3:c.3135-57T=	XP_011543810.3:n.3135-57T=
XM_011545510.2:c.2241-57T=	XP_011543812.1:n.2241-57T=
XM_011545511.2:c.1872-57T=	XP_011543813.1:n.1872-57T=
NM_001001671.4:c.3567-57T= MANE Select	NP_001001671.3:n.3567-57T=