Canonical Allele Identifier: CA1217904216

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039386_197039392delinsTTAAGGG , CM000663.2:g.197039386_197039392delinsTTAAGGG	GRCh38
NC_000001.10:g.197008516_197008522delinsTTAAGGG , CM000663.1:g.197008516_197008522delinsTTAAGGG	GRCh37
NC_000001.9:g.195275139_195275145delinsTTAAGGG	NCBI36
NG_012065.1:g.32876_32882delinsCCCTTAA , LRG_550:g.32876_32882delinsCCCTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.1972_1978delinsCCCTTAA MANE Select	ENSP00000356382.2:p.Pro658=
ENST00000649282.1:c.727_733delinsCCCTTAA	ENSP00000497116.1:p.Pro243=
ENST00000367412.1:c.1972_1978delinsCCCTTAA	ENSP00000356382.1:p.Pro658=
NM_001994.2:c.1972_1978delinsCCCTTAA , LRG_550t1:c.1972_1978delinsCCCTTAA	NP_001985.2:p.Pro658=
XM_011509283.2:c.*907_*913delinsCCCTTAA	XP_011507585.1:n.*907_*913delinsCCCTTAA
XM_011509284.2:c.*907_*913delinsCCCTTAA	XP_011507586.1:n.*907_*913delinsCCCTTAA
XM_011509286.2:c.*907_*913delinsCCCTTAA	XP_011507588.1:n.*907_*913delinsCCCTTAA
NM_001994.3:c.1972_1978delinsCCCTTAA MANE Select	NP_001985.2:p.Pro658=