Canonical Allele Identifier: CA3624827

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6318700_6318702dup , CM000668.2:g.6318700_6318702dup	GRCh38
NC_000006.11:g.6318933_6318935dup , CM000668.1:g.6318933_6318935dup	GRCh37
NC_000006.10:g.6263932_6263934dup	NCBI36
NG_008107.1:g.7001_7003dup , LRG_549:g.7001_7003dup

Transcript Alleles

HGVS	Amino-acid Change
NM_000129.4:c.-18-9_-18-7dup MANE Select	NP_000120.2:n.-18-9_-18-7dup
ENST00000264870.8:c.-18-9_-18-7dup MANE Select	ENSP00000264870.3:n.-18-9_-18-7dup
NM_000129.3:c.-18-9_-18-7dup , LRG_549t1:c.-18-9_-18-7dup	NP_000120.2:n.-18-9_-18-7dup
ENST00000264870.7:c.-18-9_-18-7dup	ENSP00000264870.3:n.-18-9_-18-7dup
ENST00000414279.5:c.-18-9_-18-7dup	ENSP00000413334.1:n.-18-9_-18-7dup
ENST00000431222.6:c.145-9_145-7dup	ENSP00000416295.2:n.145-9_145-7dup
ENST00000451619.1:c.57-9_57-7dup
XM_006715010.2:c.-18-9_-18-7dup	XP_006715073.1:n.-18-9_-18-7dup
XM_011514342.1:c.145-9_145-7dup	XP_011512644.1:n.145-9_145-7dup