Canonical Allele Identifier: CA2418227145

Gene: MAP3K15

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362844_19362845delinsCA , CM000685.2:g.19362844_19362845delinsCA	GRCh38
NC_000023.10:g.19380962_19380963delinsCA , CM000685.1:g.19380962_19380963delinsCA	GRCh37
NC_000023.9:g.19290883_19290884delinsCA	NCBI36
NG_016781.1:g.23952_23953delinsCA
NG_021184.1:g.157417_157418delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3572_3573delinsTG MANE Select	ENSP00000345629.4:p.Leu1191=
ENST00000338883.8:c.3572_3573delinsTG	ENSP00000345629.4:p.Leu1191=
ENST00000359173.7:c.2900_2901delinsTG
ENST00000470101.1:n.990_991delinsTG
ENST00000518578.5:n.3634_3635delinsTG
NM_001001671.3:c.3572_3573delinsTG	NP_001001671.3:p.Leu1191=
XM_011545507.1:c.3227_3228delinsTG	XP_011543809.1:p.Leu1076=
XM_011545508.1:c.3140_3141delinsTG	XP_011543810.1:p.Leu1047=
XM_011545509.1:c.2537_2538delinsTG	XP_011543811.1:p.Leu846=
XM_011545510.1:c.2246_2247delinsTG	XP_011543812.1:p.Leu749=
XM_011545511.1:c.1877_1878delinsTG	XP_011543813.1:p.Leu626=
XM_011545507.3:c.3227_3228delinsTG	XP_011543809.3:p.Leu1076=
XM_011545508.3:c.3140_3141delinsTG	XP_011543810.3:p.Leu1047=
XM_011545510.2:c.2246_2247delinsTG	XP_011543812.1:p.Leu749=
XM_011545511.2:c.1877_1878delinsTG	XP_011543813.1:p.Leu626=
NM_001001671.4:c.3572_3573delinsTG MANE Select	NP_001001671.3:p.Leu1191=