Canonical Allele Identifier: CA8440167

Gene: B9D1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19343841G>A , CM000679.2:g.19343841G>A	GRCh38
NC_000017.10:g.19247154G>A , CM000679.1:g.19247154G>A	GRCh37
NC_000017.9:g.19187747G>A	NCBI36
NG_031885.1:g.39342C>T
NG_031885.2:g.39353C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261499.11:c.421C>T MANE Select	ENSP00000261499.4:p.Arg141Trp
ENST00000261499.10:c.421C>T	ENSP00000261499.4:p.Arg141Trp
ENST00000477478.7:c.61C>T	ENSP00000460939.2:p.Arg21Trp
ENST00000575478.7:c.61C>T	ENSP00000458525.3:p.Arg21Trp
ENST00000582857.2:c.61C>T	ENSP00000463165.2:p.Arg21Trp
ENST00000642870.2:c.61C>T	ENSP00000496409.2:p.Arg21Trp
ENST00000646248.1:c.214C>T	ENSP00000493599.1:p.Arg72Trp
ENST00000647056.1:c.*35C>T	ENSP00000496502.1:n.*35C>T
ENST00000647252.1:c.421C>T	ENSP00000495045.1:p.Arg141Trp
ENST00000663089.1:c.484C>T	ENSP00000499469.1:p.Arg162Trp
ENST00000671102.1:c.484C>T	ENSP00000499690.1:p.Arg162Trp
ENST00000674596.1:c.246C>T	ENSP00000501877.1:p.Gly82=
ENST00000675510.1:c.404+3428C>T	ENSP00000501817.1:n.404+3428C>T
ENST00000261499.8:c.421C>T	ENSP00000261499.4:p.Arg141Trp
ENST00000395615.5:c.421C>T	ENSP00000378977.1:p.Arg141Trp
ENST00000395616.7:c.421C>T	ENSP00000378978.3:p.Arg141Trp
ENST00000461069.6:c.421C>T	ENSP00000433359.2:p.Arg141Trp
ENST00000477478.6:c.348C>T	ENSP00000460939.1:p.Gly116=
ENST00000575403.5:c.348C>T	ENSP00000459857.1:p.Gly116=
ENST00000575478.5:c.348C>T	ENSP00000458525.1:p.Gly116=
NM_001243473.1:c.480C>T	NP_001230402.1:p.Gly160=
NM_001243475.1:c.348C>T	NP_001230404.1:p.Gly116=
NM_015681.3:c.421C>T	NP_056496.1:p.Arg141Trp
XM_005256605.2:c.421C>T	XP_005256662.1:p.Arg141Trp
XM_005256607.2:c.421C>T	XP_005256664.1:p.Arg141Trp
XM_005256608.2:c.404+3428C>T	XP_005256665.1:n.404+3428C>T
XM_011523793.1:c.421C>T	XP_011522095.1:p.Arg141Trp
XM_011523794.1:c.421C>T	XP_011522096.1:p.Arg141Trp
NM_001243473.2:c.480C>T	NP_001230402.1:p.Gly160=
NM_001243475.2:c.348C>T	NP_001230404.1:p.Gly116=
NM_001321214.1:c.421C>T	NP_001308143.1:p.Arg141Trp
NM_001321215.1:c.421C>T	NP_001308144.1:p.Arg141Trp
NM_001321217.1:c.421C>T	NP_001308146.1:p.Arg141Trp
NM_001321218.1:c.421C>T	NP_001308147.1:p.Arg141Trp
NM_001321219.1:c.404+3428C>T	NP_001308148.1:n.404+3428C>T
NM_001330149.1:c.421C>T	NP_001317078.1:p.Arg141Trp
NM_015681.4:c.421C>T	NP_056496.1:p.Arg141Trp
NM_001321214.2:c.421C>T	NP_001308143.1:p.Arg141Trp
NM_001321215.2:c.421C>T	NP_001308144.1:p.Arg141Trp
NM_001321217.2:c.421C>T	NP_001308146.1:p.Arg141Trp
NM_001321218.2:c.421C>T	NP_001308147.1:p.Arg141Trp
NM_001321219.2:c.404+3428C>T	NP_001308148.1:n.404+3428C>T
NM_001368769.2:c.61C>T	NP_001355698.1:p.Arg21Trp
NM_015681.5:c.421C>T	NP_056496.1:p.Arg141Trp
NM_001321215.3:c.421C>T	NP_001308144.1:p.Arg141Trp
NM_001330149.2:c.421C>T	NP_001317078.1:p.Arg141Trp
NM_015681.6:c.421C>T MANE Select	NP_056496.1:p.Arg141Trp