Canonical Allele Identifier: CA1607973463

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182200_6182204delinsTTAAC , CM000668.2:g.6182200_6182204delinsTTAAC	GRCh38
NC_000006.11:g.6182433_6182437delinsTTAAC , CM000668.1:g.6182433_6182437delinsTTAAC	GRCh37
NC_000006.10:g.6127432_6127436delinsTTAAC	NCBI36
NG_008107.1:g.143488_143492delinsGTTAA , LRG_549:g.143488_143492delinsGTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.1306-63_1306-59delinsGTTAA MANE Select	ENSP00000264870.3:n.1306-63_1306-59delinsGTTAA
ENST00000264870.7:c.1306-63_1306-59delinsGTTAA	ENSP00000264870.3:n.1306-63_1306-59delinsGTTAA
NM_000129.3:c.1306-63_1306-59delinsGTTAA , LRG_549t1:c.1306-63_1306-59delinsGTTAA	NP_000120.2:n.1306-63_1306-59delinsGTTAA
XM_006715010.2:c.1306-63_1306-59delinsGTTAA	XP_006715073.1:n.1306-63_1306-59delinsGTTAA
XM_011514342.1:c.1468-63_1468-59delinsGTTAA	XP_011512644.1:n.1468-63_1468-59delinsGTTAA
NM_000129.4:c.1306-63_1306-59delinsGTTAA MANE Select	NP_000120.2:n.1306-63_1306-59delinsGTTAA