Canonical Allele Identifier: CA2623811606

Gene: F7

Linked Data

• gnomAD v4: 13-113119927-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119927T>C , CM000675.2:g.113119927T>C	GRCh38
NC_000013.10:g.113774241T>C , CM000675.1:g.113774241T>C	GRCh37
NC_000013.9:g.112822242T>C	NCBI36
NG_009258.1:g.2129T>C , LRG_548:g.2129T>C
NG_009262.1:g.19137T>C , LRG_554:g.19137T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.*919T>C MANE Select	ENSP00000329546.4:n.*919T>C
ENST00000346342.7:c.*919T>C	ENSP00000329546.3:n.*919T>C
ENST00000375581.3:c.*919T>C	ENSP00000364731.3:n.*919T>C
ENST00000541084.5:c.*919T>C	ENSP00000442051.2:n.*919T>C
NM_000131.4:c.*919T>C , LRG_554t1:c.*919T>C	NP_000122.1:n.*919T>C
NM_001267554.1:c.*919T>C	NP_001254483.1:n.*919T>C
NM_019616.3:c.*919T>C , LRG_554t2:c.*919T>C	NP_062562.1:n.*919T>C
NR_051961.1:n.2341T>C
XM_006719963.2:c.*919T>C	XP_006720026.1:n.*919T>C
XM_011537474.1:c.*919T>C	XP_011535776.1:n.*919T>C
XM_011537475.1:c.*919T>C	XP_011535777.1:n.*919T>C
XM_011537476.1:c.*919T>C	XP_011535778.1:n.*919T>C
XM_011537477.1:c.*919T>C	XP_011535779.1:n.*919T>C
XM_006719963.3:c.*919T>C	XP_006720026.2:n.*919T>C
XM_011537474.2:c.*919T>C	XP_011535776.2:n.*919T>C
XM_011537475.2:c.*919T>C	XP_011535777.2:n.*919T>C
XM_011537476.2:c.*919T>C	XP_011535778.1:n.*919T>C
NM_019616.4:c.*919T>C MANE Select	NP_062562.1:n.*919T>C
NR_051961.2:n.2338T>C
NM_001267554.2:c.*919T>C	NP_001254483.1:n.*919T>C