Canonical Allele Identifier: CA15519983

Gene: DOCK4

Linked Data

• dbSNP Id: rs10255299
• gnomAD v2: 7-111527560-G-A
• gnomAD v3: 7-111887504-G-A
• gnomAD v4: 7-111887504-G-A
• MyVariant Identifiers: chr7:g.111527560G>A (hg19) ; chr7:g.111887504G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.111887504G>A , CM000669.2:g.111887504G>A	GRCh38
NC_000007.13:g.111527560G>A , CM000669.1:g.111527560G>A	GRCh37
NC_000007.12:g.111314796G>A	NCBI36
NG_028060.1:g.323903C>T
NG_028060.2:g.323908C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000428084.6:c.1587+8108C>T MANE Select	ENSP00000410746.1:n.1587+8108C>T
ENST00000437633.6:c.1587+8108C>T	ENSP00000404179.1:n.1587+8108C>T
ENST00000494651.7:c.1551+8108C>T	ENSP00000440944.3:n.1551+8108C>T
ENST00000428084.5:c.1587+8108C>T	ENSP00000410746.1:n.1587+8108C>T
ENST00000437633.5:c.1587+8108C>T	ENSP00000404179.1:n.1587+8108C>T
ENST00000445943.5:c.1550+8108C>T
ENST00000476846.5:n.1843+8108C>T
ENST00000494651.6:c.1551+8108C>T	ENSP00000440944.2:n.1551+8108C>T
NM_014705.3:c.1587+8108C>T	NP_055520.3:n.1587+8108C>T
XM_006716188.1:c.1587+8108C>T	XP_006716251.1:n.1587+8108C>T
XM_006716189.1:c.1587+8108C>T	XP_006716252.1:n.1587+8108C>T
XM_011516716.1:c.1587+8108C>T	XP_011515018.1:n.1587+8108C>T
XM_011516717.1:c.1587+8108C>T	XP_011515019.1:n.1587+8108C>T
NM_001363540.1:c.1587+8108C>T	NP_001350469.1:n.1587+8108C>T
XM_006716189.2:c.1587+8108C>T	XP_006716252.1:n.1587+8108C>T
XM_017012819.1:c.1680+8108C>T	XP_016868308.1:n.1680+8108C>T
XM_017012820.1:c.1680+8108C>T	XP_016868309.1:n.1680+8108C>T
XM_017012821.1:c.1680+8108C>T	XP_016868310.1:n.1680+8108C>T
XM_017012822.1:c.1620+8108C>T	XP_016868311.1:n.1620+8108C>T
XM_017012823.1:c.1680+8108C>T	XP_016868312.1:n.1680+8108C>T
XM_017012824.1:c.1680+8108C>T	XP_016868313.1:n.1680+8108C>T
XM_017012825.1:c.1680+8108C>T	XP_016868314.1:n.1680+8108C>T
XM_024447006.1:c.1359+8108C>T	XP_024302774.1:n.1359+8108C>T
NM_014705.4:c.1587+8108C>T	NP_055520.3:n.1587+8108C>T
NM_001363540.2:c.1587+8108C>T MANE Select	NP_001350469.1:n.1587+8108C>T