Canonical Allele Identifier: CA2819936202

Gene: MAP3K15

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362853_19362855del , CM000685.2:g.19362853_19362855del	GRCh38
NC_000023.10:g.19380971_19380973del , CM000685.1:g.19380971_19380973del	GRCh37
NC_000023.9:g.19290892_19290894del	NCBI36
NG_016781.1:g.23961_23963del
NG_021184.1:g.157408_157410del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3567-4_3567-2del MANE Select	ENSP00000345629.4:n.3567-4_3567-2del
ENST00000338883.8:c.3567-4_3567-2del	ENSP00000345629.4:n.3567-4_3567-2del
ENST00000359173.7:c.2895-4_2895-2del
ENST00000470101.1:n.985-4_985-2del
ENST00000518578.5:n.3629-4_3629-2del
NM_001001671.3:c.3567-4_3567-2del	NP_001001671.3:n.3567-4_3567-2del
XM_011545507.1:c.3222-4_3222-2del	XP_011543809.1:n.3222-4_3222-2del
XM_011545508.1:c.3135-4_3135-2del	XP_011543810.1:n.3135-4_3135-2del
XM_011545509.1:c.2532-4_2532-2del	XP_011543811.1:n.2532-4_2532-2del
XM_011545510.1:c.2241-4_2241-2del	XP_011543812.1:n.2241-4_2241-2del
XM_011545511.1:c.1872-4_1872-2del	XP_011543813.1:n.1872-4_1872-2del
XM_011545507.3:c.3222-4_3222-2del	XP_011543809.3:n.3222-4_3222-2del
XM_011545508.3:c.3135-4_3135-2del	XP_011543810.3:n.3135-4_3135-2del
XM_011545510.2:c.2241-4_2241-2del	XP_011543812.1:n.2241-4_2241-2del
XM_011545511.2:c.1872-4_1872-2del	XP_011543813.1:n.1872-4_1872-2del
NM_001001671.4:c.3567-4_3567-2del MANE Select	NP_001001671.3:n.3567-4_3567-2del