Canonical Allele Identifier: CA1140532807

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197055729_197055732delinsGGGG , CM000663.2:g.197055729_197055732delinsGGGG	GRCh38
NC_000001.10:g.197024859_197024862delinsGGGG , CM000663.1:g.197024859_197024862delinsGGGG	GRCh37
NC_000001.9:g.195291482_195291485delinsGGGG	NCBI36
NG_012065.1:g.16536_16539delinsCCCC , LRG_550:g.16536_16539delinsCCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1337_1340delinsCCCC MANE Select	ENSP00000356382.2:p.Ser446=
ENST00000649282.1:c.92_95delinsCCCC	ENSP00000497116.1:p.Ser31=
ENST00000367412.1:c.1337_1340delinsCCCC	ENSP00000356382.1:p.Ser446=
NM_001994.2:c.1337_1340delinsCCCC , LRG_550t1:c.1337_1340delinsCCCC	NP_001985.2:p.Ser446=
XM_011509283.1:c.1337_1340delinsCCCC	XP_011507585.1:p.Ser446=
XM_011509284.1:c.1334_1337delinsCCCC	XP_011507586.1:p.Ser445=
XM_011509285.1:c.1241_1244delinsCCCC	XP_011507587.1:p.Ser414=
XM_011509286.1:c.1193_1196delinsCCCC	XP_011507588.1:p.Ser398=
XM_011509283.2:c.1337_1340delinsCCCC	XP_011507585.1:p.Ser446=
XM_011509284.2:c.1334_1337delinsCCCC	XP_011507586.1:p.Ser445=
XM_011509286.2:c.1193_1196delinsCCCC	XP_011507588.1:p.Ser398=
NM_001994.3:c.1337_1340delinsCCCC MANE Select	NP_001985.2:p.Ser446=