Canonical Allele Identifier: CA327034329

Gene: MAP3K15

Linked Data

• dbSNP Id: rs780729897
• gnomAD v3: X-19362913-C-G
• gnomAD v4: X-19362913-C-G
• MyVariant Identifiers: chrX:g.19381031C>G (hg19) ; chrX:g.19362913C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19362913C>G , CM000685.2:g.19362913C>G	GRCh38
NC_000023.10:g.19381031C>G , CM000685.1:g.19381031C>G	GRCh37
NC_000023.9:g.19290952C>G	NCBI36
NG_016781.1:g.24021C>G
NG_021184.1:g.157349G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338883.9:c.3567-63G>C MANE Select	ENSP00000345629.4:n.3567-63G>C
ENST00000338883.8:c.3567-63G>C	ENSP00000345629.4:n.3567-63G>C
ENST00000359173.7:c.2895-63G>C
ENST00000470101.1:n.985-63G>C
ENST00000518578.5:n.3629-63G>C
NM_001001671.3:c.3567-63G>C	NP_001001671.3:n.3567-63G>C
XM_011545507.1:c.3222-63G>C	XP_011543809.1:n.3222-63G>C
XM_011545508.1:c.3135-63G>C	XP_011543810.1:n.3135-63G>C
XM_011545509.1:c.2532-63G>C	XP_011543811.1:n.2532-63G>C
XM_011545510.1:c.2241-63G>C	XP_011543812.1:n.2241-63G>C
XM_011545511.1:c.1872-63G>C	XP_011543813.1:n.1872-63G>C
XM_011545507.3:c.3222-63G>C	XP_011543809.3:n.3222-63G>C
XM_011545508.3:c.3135-63G>C	XP_011543810.3:n.3135-63G>C
XM_011545510.2:c.2241-63G>C	XP_011543812.1:n.2241-63G>C
XM_011545511.2:c.1872-63G>C	XP_011543813.1:n.1872-63G>C
NM_001001671.4:c.3567-63G>C MANE Select	NP_001001671.3:n.3567-63G>C