Canonical Allele Identifier: CA1607991964

Gene: F13A1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6283433G>A , CM000668.2:g.6283433G>A	GRCh38
NC_000006.11:g.6283666G>A , CM000668.1:g.6283666G>A	GRCh37
NC_000006.10:g.6228665G>A	NCBI36
NG_008107.1:g.42259C>T , LRG_549:g.42259C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.320-16624C>T MANE Select	ENSP00000264870.3:n.320-16624C>T
ENST00000264870.7:c.320-16624C>T	ENSP00000264870.3:n.320-16624C>T
ENST00000414279.5:c.320-16624C>T	ENSP00000413334.1:n.320-16624C>T
ENST00000431222.6:c.482-16624C>T	ENSP00000416295.2:n.482-16624C>T
ENST00000479211.1:n.305-16624C>T
NM_000129.3:c.320-16624C>T , LRG_549t1:c.320-16624C>T	NP_000120.2:n.320-16624C>T
XM_006715010.2:c.320-16624C>T	XP_006715073.1:n.320-16624C>T
XM_011514342.1:c.482-16624C>T	XP_011512644.1:n.482-16624C>T
NM_000129.4:c.320-16624C>T MANE Select	NP_000120.2:n.320-16624C>T