Canonical Allele Identifier: CA15460307
Gene: DAAM2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2395730

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39816589C>A , CM000668.2:g.39816589C>A GRCh38
NC_000006.11:g.39784365C>A , CM000668.1:g.39784365C>A GRCh37
NC_000006.10:g.39892343C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001201427.1:c.-57+24124C>A VV NP_001188356.1:p.=
NM_015345.3:c.-57+23446C>A VV NP_056160.2:p.=
XM_006715043.1:c.-57+24124C>A XP_006715106.1:p.=
XM_006715046.2:c.-57+23446C>A XP_006715109.1:p.=
XR_926775.1:n.38+3108G>T
XM_006715043.2:c.-57+24124C>A XP_006715106.1:p.=
XM_006715046.4:c.-57+23446C>A XP_006715109.1:p.=
XM_017010630.1:c.13+21838C>A XP_016866119.1:p.=
NM_001201427.2:c.-57+24124C>A VV MANE Preferred NP_001188356.1:p.=
ENST00000274867.8:c.-57+24124C>A ENSP00000274867.4:p.=
ENST00000398904.6:c.-57+23446C>A ENSP00000381876.2:p.=
ENST00000475489.5:n.70+24124C>A
ENST00000491083.2:n.90+24124C>A
ENST00000494405.2:c.-57+24124C>A ENSP00000488196.1:p.=
ENST00000538976.5:c.-57+23446C>A ENSP00000437808.1:p.=
ENST00000633794.1:c.-57+24124C>A ENSP00000488831.1:p.=