Canonical Allele Identifier: CA2693252653

Gene: MAP3K15

Linked Data

• gnomAD v4: X-19362857-T-TAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362869_19362874dup , CM000685.2:g.19362869_19362874dup	GRCh38
NC_000023.10:g.19380987_19380992dup , CM000685.1:g.19380987_19380992dup	GRCh37
NC_000023.9:g.19290908_19290913dup	NCBI36
NG_016781.1:g.23977_23982dup
NG_021184.1:g.157399_157404dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3567-13_3567-8dup MANE Select	ENSP00000345629.4:n.3567-13_3567-8dup
ENST00000338883.8:c.3567-13_3567-8dup	ENSP00000345629.4:n.3567-13_3567-8dup
ENST00000359173.7:c.2895-13_2895-8dup
ENST00000470101.1:n.985-13_985-8dup
ENST00000518578.5:n.3629-13_3629-8dup
NM_001001671.3:c.3567-13_3567-8dup	NP_001001671.3:n.3567-13_3567-8dup
XM_011545507.1:c.3222-13_3222-8dup	XP_011543809.1:n.3222-13_3222-8dup
XM_011545508.1:c.3135-13_3135-8dup	XP_011543810.1:n.3135-13_3135-8dup
XM_011545509.1:c.2532-13_2532-8dup	XP_011543811.1:n.2532-13_2532-8dup
XM_011545510.1:c.2241-13_2241-8dup	XP_011543812.1:n.2241-13_2241-8dup
XM_011545511.1:c.1872-13_1872-8dup	XP_011543813.1:n.1872-13_1872-8dup
XM_011545507.3:c.3222-13_3222-8dup	XP_011543809.3:n.3222-13_3222-8dup
XM_011545508.3:c.3135-13_3135-8dup	XP_011543810.3:n.3135-13_3135-8dup
XM_011545510.2:c.2241-13_2241-8dup	XP_011543812.1:n.2241-13_2241-8dup
XM_011545511.2:c.1872-13_1872-8dup	XP_011543813.1:n.1872-13_1872-8dup
NM_001001671.4:c.3567-13_3567-8dup MANE Select	NP_001001671.3:n.3567-13_3567-8dup