Canonical Allele Identifier: CA1367315

Gene: C4BPB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207096574C>T , CM000663.2:g.207096574C>T	GRCh38
NC_000001.10:g.207269919C>T , CM000663.1:g.207269919C>T	GRCh37
NC_000001.9:g.205336542C>T	NCBI36
NG_029386.1:g.12708C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001017365.3:c.462C>T MANE Select	NP_001017365.1:p.Asn154=
ENST00000367078.8:c.462C>T MANE Select	ENSP00000356045.3:p.Asn154=
NM_000716.3:c.462C>T	NP_000707.1:p.Asn154=
NM_001017364.1:c.459C>T	NP_001017364.1:p.Asn153=
NM_001017365.1:c.462C>T	NP_001017365.1:p.Asn154=
NM_001017365.2:c.462C>T	NP_001017365.1:p.Asn154=
NM_001017366.1:c.459C>T	NP_001017366.1:p.Asn153=
NM_001017366.2:c.459C>T	NP_001017366.1:p.Asn153=
NM_001017366.3:c.459C>T	NP_001017366.1:p.Asn153=
NM_001017367.1:c.462C>T	NP_001017367.1:p.Asn154=
ENST00000243611.9:c.462C>T	ENSP00000243611.5:p.Asn154=
ENST00000367076.7:c.459C>T	ENSP00000356043.3:p.Asn153=
ENST00000367078.7:c.462C>T	ENSP00000356045.3:p.Asn154=
ENST00000391923.1:c.462C>T	ENSP00000375790.1:p.Asn154=
ENST00000452902.6:c.462C>T	ENSP00000392237.1:p.Asn154=
ENST00000469326.1:n.1641C>T
XM_005273253.3:c.462C>T	XP_005273310.1:p.Asn154=
XM_005273254.3:c.462C>T	XP_005273311.1:p.Asn154=
XM_005273254.5:c.462C>T	XP_005273311.1:p.Asn154=
XM_024449464.1:c.459C>T	XP_024305232.1:p.Asn153=