Canonical Allele Identifier: CA388787182

Gene: F7

Linked Data

• gnomAD v4: 13-113118970-C-T
• MyVariant Identifiers: chr13:g.113773284C>T (hg19) ; chr13:g.113118970C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118970C>T , CM000675.2:g.113118970C>T	GRCh38
NC_000013.10:g.113773284C>T , CM000675.1:g.113773284C>T	GRCh37
NC_000013.9:g.112821285C>T	NCBI36
NG_009258.1:g.1172C>T , LRG_548:g.1172C>T
NG_009262.1:g.18180C>T , LRG_554:g.18180C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1297C>T MANE Select	ENSP00000329546.4:p.Pro433Ser
ENST00000346342.7:c.1297C>T	ENSP00000329546.3:p.Pro433Ser
ENST00000375581.3:c.1363C>T	ENSP00000364731.3:p.Pro455Ser
ENST00000541084.5:c.1111C>T	ENSP00000442051.2:p.Pro371Ser
NM_000131.4:c.1363C>T , LRG_554t1:c.1363C>T	NP_000122.1:p.Pro455Ser
NM_001267554.1:c.1111C>T	NP_001254483.1:p.Pro371Ser
NM_019616.3:c.1297C>T , LRG_554t2:c.1297C>T	NP_062562.1:p.Pro433Ser
NR_051961.1:n.1384C>T
XM_006719963.2:c.1156C>T	XP_006720026.1:p.Pro386Ser
XM_011537474.1:c.1405C>T	XP_011535776.1:p.Pro469Ser
XM_011537475.1:c.1219C>T	XP_011535777.1:p.Pro407Ser
XM_011537476.1:c.1057C>T	XP_011535778.1:p.Pro353Ser
XM_011537477.1:c.1366C>T	XP_011535779.1:p.Pro456Ser
XM_006719963.3:c.1201C>T	XP_006720026.2:p.Pro401Ser
XM_011537474.2:c.1450C>T	XP_011535776.2:p.Pro484Ser
XM_011537475.2:c.1264C>T	XP_011535777.2:p.Pro422Ser
XM_011537476.2:c.1057C>T	XP_011535778.1:p.Pro353Ser
NM_019616.4:c.1297C>T MANE Select	NP_062562.1:p.Pro433Ser
NR_051961.2:n.1381C>T
NM_001267554.2:c.1111C>T	NP_001254483.1:p.Pro371Ser