Canonical Allele Identifier: CA1622844549

Gene: DAAM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39816627T= , CM000668.2:g.39816627T=	GRCh38
NC_000006.11:g.39784403T= , CM000668.1:g.39784403T=	GRCh37
NC_000006.10:g.39892381T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000274867.9:c.-57+24162T= MANE Select	ENSP00000274867.4:n.-57+24162T=
ENST00000274867.8:c.-57+24162T=	ENSP00000274867.4:n.-57+24162T=
ENST00000398904.6:c.-57+23484T=	ENSP00000381876.2:n.-57+23484T=
ENST00000475489.5:n.70+24162T=
ENST00000491083.2:n.90+24162T=
ENST00000494405.2:c.-57+24162T=	ENSP00000488196.1:n.-57+24162T=
ENST00000538976.5:c.-57+23484T=	ENSP00000437808.1:n.-57+23484T=
ENST00000633794.1:c.-57+24162T=	ENSP00000488831.1:n.-57+24162T=
NM_001201427.1:c.-57+24162T=	NP_001188356.1:n.-57+24162T=
NM_015345.3:c.-57+23484T=	NP_056160.2:n.-57+23484T=
XM_006715043.1:c.-57+24162T=	XP_006715106.1:n.-57+24162T=
XM_006715046.2:c.-57+23484T=	XP_006715109.1:n.-57+23484T=
XR_926775.1:n.38+3070A=
XM_006715043.2:c.-57+24162T=	XP_006715106.1:n.-57+24162T=
XM_006715046.4:c.-57+23484T=	XP_006715109.1:n.-57+23484T=
XM_017010630.1:c.13+21876T=	XP_016866119.1:n.13+21876T=
NM_001201427.2:c.-57+24162T= MANE Select	NP_001188356.1:n.-57+24162T=
NM_015345.4:c.-57+23484T=	NP_056160.2:n.-57+23484T=