Canonical Allele Identifier: CA2418227108

Gene: MAP3K15

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362751T= , CM000685.2:g.19362751T=	GRCh38
NC_000023.10:g.19380869T= , CM000685.1:g.19380869T=	GRCh37
NC_000023.9:g.19290790T=	NCBI36
NG_016781.1:g.23859T=
NG_021184.1:g.157511A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3666A= MANE Select	ENSP00000345629.4:p.Lys1222=
ENST00000338883.8:c.3666A=	ENSP00000345629.4:p.Lys1222=
ENST00000359173.7:c.2994A=
ENST00000470101.1:n.1084A=
ENST00000518578.5:n.3728A=
NM_001001671.3:c.3666A=	NP_001001671.3:p.Lys1222=
XM_011545507.1:c.3321A=	XP_011543809.1:p.Lys1107=
XM_011545508.1:c.3234A=	XP_011543810.1:p.Lys1078=
XM_011545509.1:c.2631A=	XP_011543811.1:p.Lys877=
XM_011545510.1:c.2340A=	XP_011543812.1:p.Lys780=
XM_011545511.1:c.1971A=	XP_011543813.1:p.Lys657=
XM_011545507.3:c.3321A=	XP_011543809.3:p.Lys1107=
XM_011545508.3:c.3234A=	XP_011543810.3:p.Lys1078=
XM_011545510.2:c.2340A=	XP_011543812.1:p.Lys780=
XM_011545511.2:c.1971A=	XP_011543813.1:p.Lys657=
NM_001001671.4:c.3666A= MANE Select	NP_001001671.3:p.Lys1222=