Canonical Allele Identifier: CA15610377

Gene: MAPKAP1

Linked Data

• dbSNP Id: rs536861
• gnomAD v2: 9-128313444-A-C
• gnomAD v3: 9-125551165-A-C
• gnomAD v4: 9-125551165-A-C
• MyVariant Identifiers: chr9:g.128313444A>C (hg19) ; chr9:g.125551165A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125551165A>C , CM000671.2:g.125551165A>C	GRCh38
NC_000009.11:g.128313444A>C , CM000671.1:g.128313444A>C	GRCh37
NC_000009.10:g.127353265A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265960.8:c.849-7997T>G MANE Select	ENSP00000265960.3:n.849-7997T>G
ENST00000265960.7:c.849-7997T>G	ENSP00000265960.3:n.849-7997T>G
ENST00000350766.7:c.849-7997T>G	ENSP00000265961.5:n.849-7997T>G
ENST00000373498.5:c.849-7997T>G	ENSP00000362597.1:n.849-7997T>G
ENST00000373503.7:c.273-7997T>G	ENSP00000362602.3:n.273-7997T>G
ENST00000373511.6:c.849-7997T>G	ENSP00000362610.2:n.849-7997T>G
ENST00000394060.7:c.849-7997T>G	ENSP00000377624.3:n.849-7997T>G
ENST00000394063.5:c.273-7997T>G	ENSP00000377627.1:n.273-7997T>G
ENST00000420643.5:c.273-7997T>G	ENSP00000400182.1:n.273-7997T>G
ENST00000427078.5:c.273-7997T>G	ENSP00000408359.1:n.273-7997T>G
ENST00000473837.5:n.449-7997T>G
ENST00000497932.5:c.273-7997T>G	ENSP00000418607.1:n.273-7997T>G
NM_001006617.1:c.849-7997T>G	NP_001006618.1:n.849-7997T>G
NM_001006618.1:c.849-7997T>G	NP_001006619.1:n.849-7997T>G
NM_001006619.1:c.849-7997T>G	NP_001006620.1:n.849-7997T>G
NM_001006620.1:c.273-7997T>G	NP_001006621.1:n.273-7997T>G
NM_001006621.1:c.273-7997T>G	NP_001006622.1:n.273-7997T>G
NM_024117.3:c.849-7997T>G	NP_077022.1:n.849-7997T>G
XM_011519005.1:c.990-7997T>G	XP_011517307.1:n.990-7997T>G
XM_011519006.1:c.990-7997T>G	XP_011517308.1:n.990-7997T>G
XM_011519007.1:c.990-7997T>G	XP_011517309.1:n.990-7997T>G
XM_011519008.1:c.990-7997T>G	XP_011517310.1:n.990-7997T>G
XM_011519009.1:c.990-7997T>G	XP_011517311.1:n.990-7997T>G
XM_011519010.1:c.273-7997T>G	XP_011517312.1:n.273-7997T>G
XR_930351.1:n.6583A>C
XR_930352.1:n.1908-39A>C
XR_930353.1:n.1910-4687A>C
XR_930354.1:n.1908-2577A>C
XM_011519005.2:c.990-7997T>G	XP_011517307.1:n.990-7997T>G
XM_011519006.3:c.990-7997T>G	XP_011517308.1:n.990-7997T>G
XM_011519010.2:c.273-7997T>G	XP_011517312.1:n.273-7997T>G
XM_017015126.1:c.849-7997T>G	XP_016870615.1:n.849-7997T>G
XM_017015127.1:c.849-7997T>G	XP_016870616.1:n.849-7997T>G
XM_024447670.1:c.849-7997T>G	XP_024303438.1:n.849-7997T>G
XR_001746932.1:n.179-39A>C
XR_001746933.1:n.537-39A>C
NM_001006617.2:c.849-7997T>G	NP_001006618.1:n.849-7997T>G
NM_001006617.3:c.849-7997T>G MANE Select	NP_001006618.1:n.849-7997T>G
NM_001006618.2:c.849-7997T>G	NP_001006619.1:n.849-7997T>G
NM_001006619.2:c.849-7997T>G	NP_001006620.1:n.849-7997T>G
NM_001006620.2:c.273-7997T>G	NP_001006621.1:n.273-7997T>G
NM_001006621.2:c.273-7997T>G	NP_001006622.1:n.273-7997T>G
NM_024117.4:c.849-7997T>G	NP_077022.1:n.849-7997T>G