Canonical Allele Identifier: CA1217904133
Gene: F13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197039122_197039125delinsTATG , CM000663.2:g.197039122_197039125delinsTATG GRCh38
NC_000001.10:g.197008252_197008255delinsTATG , CM000663.1:g.197008252_197008255delinsTATG GRCh37
NC_000001.9:g.195274875_195274878delinsTATG NCBI36
NG_012065.1:g.33143_33146delinsCATA , LRG_550:g.33143_33146delinsCATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367412.2:c.*253_*256delinsCATA MANE Select ENSP00000356382.2:n.*253_*256delinsCATA
ENST00000649282.1:c.994_997delinsCATA ENSP00000497116.1:n.994_997delinsCATA
XM_011509283.2:c.*1174_*1177delinsCATA XP_011507585.1:n.*1174_*1177delinsCATA
XM_011509284.2:c.*1174_*1177delinsCATA XP_011507586.1:n.*1174_*1177delinsCATA
XM_011509286.2:c.*1174_*1177delinsCATA XP_011507588.1:n.*1174_*1177delinsCATA
NM_001994.3:c.*253_*256delinsCATA MANE Select NP_001985.2:n.*253_*256delinsCATA
Search 100 bp 5'
Search 100 bp 3'