Canonical Allele Identifier: CA1622844578
Gene: DAAM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39816709C= , CM000668.2:g.39816709C= GRCh38
NC_000006.11:g.39784485C= , CM000668.1:g.39784485C= GRCh37
NC_000006.10:g.39892463C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274867.9:c.-57+24244C= MANE Select ENSP00000274867.4:n.-57+24244C=
ENST00000274867.8:c.-57+24244C= ENSP00000274867.4:n.-57+24244C=
ENST00000398904.6:c.-57+23566C= ENSP00000381876.2:n.-57+23566C=
ENST00000475489.5:n.70+24244C=
ENST00000491083.2:n.90+24244C=
ENST00000494405.2:c.-57+24244C= ENSP00000488196.1:n.-57+24244C=
ENST00000538976.5:c.-57+23566C= ENSP00000437808.1:n.-57+23566C=
ENST00000633794.1:c.-57+24244C= ENSP00000488831.1:n.-57+24244C=
NM_001201427.1:c.-57+24244C= NP_001188356.1:n.-57+24244C=
NM_015345.3:c.-57+23566C= NP_056160.2:n.-57+23566C=
XM_006715043.1:c.-57+24244C= XP_006715106.1:n.-57+24244C=
XM_006715046.2:c.-57+23566C= XP_006715109.1:n.-57+23566C=
XR_926775.1:n.38+2988G=
XM_006715043.2:c.-57+24244C= XP_006715106.1:n.-57+24244C=
XM_006715046.4:c.-57+23566C= XP_006715109.1:n.-57+23566C=
XM_017010630.1:c.13+21958C= XP_016866119.1:n.13+21958C=
NM_001201427.2:c.-57+24244C= MANE Select NP_001188356.1:n.-57+24244C=
NM_015345.4:c.-57+23566C= NP_056160.2:n.-57+23566C=