Canonical Allele Identifier: CA3895186

Gene: FILIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75312825G>A , CM000668.2:g.75312825G>A	GRCh38
NC_000006.11:g.76022541G>A , CM000668.1:g.76022541G>A	GRCh37
NC_000006.10:g.76079261G>A	NCBI36
NG_051931.1:g.186090C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015687.5:c.3007C>T MANE Select	NP_056502.1:p.Pro1003Ser
ENST00000237172.12:c.3007C>T MANE Select	ENSP00000237172.7:p.Pro1003Ser
NM_001289987.1:c.3016C>T	NP_001276916.1:p.Pro1006Ser
NM_001289987.2:c.3016C>T	NP_001276916.1:p.Pro1006Ser
NM_001289987.3:c.3016C>T	NP_001276916.1:p.Pro1006Ser
NM_001300866.1:c.3007C>T	NP_001287795.1:p.Pro1003Ser
NM_001300866.2:c.3007C>T	NP_001287795.1:p.Pro1003Ser
NM_001300866.3:c.3007C>T	NP_001287795.1:p.Pro1003Ser
NM_015687.3:c.3007C>T	NP_056502.1:p.Pro1003Ser
NM_015687.4:c.3007C>T	NP_056502.1:p.Pro1003Ser
ENST00000237172.11:c.3007C>T	ENSP00000237172.7:p.Pro1003Ser
ENST00000370020.1:c.2710C>T	ENSP00000359037.1:p.Pro904Ser
ENST00000393004.6:c.3007C>T	ENSP00000376728.1:p.Pro1003Ser
ENST00000498523.1:n.2526C>T
XM_005248713.2:c.3007C>T	XP_005248770.1:p.Pro1003Ser
XM_005248713.4:c.3007C>T	XP_005248770.1:p.Pro1003Ser
XM_005248715.3:c.3007C>T	XP_005248772.1:p.Pro1003Ser
XM_005248715.5:c.3007C>T	XP_005248772.1:p.Pro1003Ser
XM_011535756.1:c.2263C>T	XP_011534058.1:p.Pro755Ser
XM_011535756.2:c.2263C>T	XP_011534058.1:p.Pro755Ser