Canonical Allele Identifier: CA15603254

Gene: MAPKAP1

Linked Data

• dbSNP Id: rs10986769
• gnomAD v2: 9-128222340-A-G
• gnomAD v3: 9-125460061-A-G
• gnomAD v4: 9-125460061-A-G
• MyVariant Identifiers: chr9:g.128222340A>G (hg19) ; chr9:g.125460061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125460061A>G , CM000671.2:g.125460061A>G	GRCh38
NC_000009.11:g.128222340A>G , CM000671.1:g.128222340A>G	GRCh37
NC_000009.10:g.127262161A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265960.8:c.1345+7911T>C MANE Select	ENSP00000265960.3:n.1345+7911T>C
ENST00000265960.7:c.1345+7911T>C	ENSP00000265960.3:n.1345+7911T>C
ENST00000350766.7:c.1237+7911T>C	ENSP00000265961.5:n.1237+7911T>C
ENST00000373498.5:c.1345+7911T>C	ENSP00000362597.1:n.1345+7911T>C
ENST00000373503.7:c.769+7911T>C	ENSP00000362602.3:n.769+7911T>C
ENST00000373511.6:c.1204+7911T>C	ENSP00000362610.2:n.1204+7911T>C
ENST00000394063.5:c.769+7911T>C	ENSP00000377627.1:n.769+7911T>C
ENST00000420643.5:c.661+7911T>C	ENSP00000400182.1:n.661+7911T>C
ENST00000444226.1:c.60-15463T>C
ENST00000483937.5:n.961+7911T>C
ENST00000496063.1:n.594+7911T>C
ENST00000497932.5:c.661+7911T>C	ENSP00000418607.1:n.661+7911T>C
NM_001006617.1:c.1345+7911T>C	NP_001006618.1:n.1345+7911T>C
NM_001006619.1:c.1204+7911T>C	NP_001006620.1:n.1204+7911T>C
NM_001006620.1:c.769+7911T>C	NP_001006621.1:n.769+7911T>C
NM_001006621.1:c.769+7911T>C	NP_001006622.1:n.769+7911T>C
NM_024117.3:c.1237+7911T>C	NP_077022.1:n.1237+7911T>C
XM_011519005.1:c.1486+7911T>C	XP_011517307.1:n.1486+7911T>C
XM_011519006.1:c.1378+7911T>C	XP_011517308.1:n.1378+7911T>C
XM_011519007.1:c.1345+7911T>C	XP_011517309.1:n.1345+7911T>C
XM_011519010.1:c.769+7911T>C	XP_011517312.1:n.769+7911T>C
XM_011519005.2:c.1486+7911T>C	XP_011517307.1:n.1486+7911T>C
XM_011519006.3:c.1378+7911T>C	XP_011517308.1:n.1378+7911T>C
XM_011519010.2:c.769+7911T>C	XP_011517312.1:n.769+7911T>C
XM_017015126.1:c.1345+7911T>C	XP_016870615.1:n.1345+7911T>C
XM_017015127.1:c.1237+7911T>C	XP_016870616.1:n.1237+7911T>C
NM_001006617.2:c.1345+7911T>C	NP_001006618.1:n.1345+7911T>C
NM_001006617.3:c.1345+7911T>C MANE Select	NP_001006618.1:n.1345+7911T>C
NM_001006619.2:c.1204+7911T>C	NP_001006620.1:n.1204+7911T>C
NM_001006620.2:c.769+7911T>C	NP_001006621.1:n.769+7911T>C
NM_001006621.2:c.769+7911T>C	NP_001006622.1:n.769+7911T>C
NM_024117.4:c.1237+7911T>C	NP_077022.1:n.1237+7911T>C