Canonical Allele Identifier: CA388786181

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772940T>C (hg19) ; chr13:g.113118626T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118626T>C , CM000675.2:g.113118626T>C	GRCh38
NC_000013.10:g.113772940T>C , CM000675.1:g.113772940T>C	GRCh37
NC_000013.9:g.112820941T>C	NCBI36
NG_009258.1:g.828T>C , LRG_548:g.828T>C
NG_009262.1:g.17836T>C , LRG_554:g.17836T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.953T>C MANE Select	ENSP00000329546.4:p.Leu318Ser
ENST00000346342.7:c.953T>C	ENSP00000329546.3:p.Leu318Ser
ENST00000375581.3:c.1019T>C	ENSP00000364731.3:p.Leu340Ser
ENST00000541084.5:c.767T>C	ENSP00000442051.2:p.Leu256Ser
NM_000131.4:c.1019T>C , LRG_554t1:c.1019T>C	NP_000122.1:p.Leu340Ser
NM_001267554.1:c.767T>C	NP_001254483.1:p.Leu256Ser
NM_019616.3:c.953T>C , LRG_554t2:c.953T>C	NP_062562.1:p.Leu318Ser
NR_051961.1:n.1040T>C
XM_006719963.2:c.812T>C	XP_006720026.1:p.Leu271Ser
XM_011537474.1:c.1061T>C	XP_011535776.1:p.Leu354Ser
XM_011537475.1:c.875T>C	XP_011535777.1:p.Leu292Ser
XM_011537476.1:c.713T>C	XP_011535778.1:p.Leu238Ser
XM_011537477.1:c.1022T>C	XP_011535779.1:p.Leu341Ser
XM_006719963.3:c.857T>C	XP_006720026.2:p.Leu286Ser
XM_011537474.2:c.1106T>C	XP_011535776.2:p.Leu369Ser
XM_011537475.2:c.920T>C	XP_011535777.2:p.Leu307Ser
XM_011537476.2:c.713T>C	XP_011535778.1:p.Leu238Ser
NM_019616.4:c.953T>C MANE Select	NP_062562.1:p.Leu318Ser
NR_051961.2:n.1037T>C
NM_001267554.2:c.767T>C	NP_001254483.1:p.Leu256Ser