Canonical Allele Identifier: CA388782421

Gene: F7

Linked Data

• gnomAD v4: 13-113113930-C-T
• COSMIC: COSM5920589 ; COSM5920590
• MyVariant Identifiers: chr13:g.113768244C>T (hg19) ; chr13:g.113113930C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113930C>T , CM000675.2:g.113113930C>T	GRCh38
NC_000013.10:g.113768244C>T , CM000675.1:g.113768244C>T	GRCh37
NC_000013.9:g.112816245C>T	NCBI36
NG_009262.1:g.13140C>T , LRG_554:g.13140C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.334C>T MANE Select	ENSP00000329546.4:p.Pro112Ser
ENST00000346342.7:c.334C>T	ENSP00000329546.3:p.Pro112Ser
ENST00000375581.3:c.400C>T	ENSP00000364731.3:p.Pro134Ser
ENST00000444337.1:c.*142C>T	ENSP00000387669.1:n.*142C>T
ENST00000473085.1:n.281C>T
ENST00000479674.1:n.667C>T
ENST00000541084.5:c.148C>T	ENSP00000442051.2:p.Pro50Ser
NM_000131.4:c.400C>T , LRG_554t1:c.400C>T	NP_000122.1:p.Pro134Ser
NM_001267554.1:c.148C>T	NP_001254483.1:p.Pro50Ser
NM_019616.3:c.334C>T , LRG_554t2:c.334C>T	NP_062562.1:p.Pro112Ser
NR_051961.1:n.421C>T
XM_006719963.2:c.334C>T	XP_006720026.1:p.Pro112Ser
XM_011537474.1:c.334C>T	XP_011535776.1:p.Pro112Ser
XM_011537475.1:c.148C>T	XP_011535777.1:p.Pro50Ser
XM_011537477.1:c.295C>T	XP_011535779.1:p.Pro99Ser
XM_006719963.3:c.379C>T	XP_006720026.2:p.Pro127Ser
XM_011537474.2:c.379C>T	XP_011535776.2:p.Pro127Ser
XM_011537475.2:c.193C>T	XP_011535777.2:p.Pro65Ser
NM_019616.4:c.334C>T MANE Select	NP_062562.1:p.Pro112Ser
NR_051961.2:n.418C>T
NM_001267554.2:c.148C>T	NP_001254483.1:p.Pro50Ser