Canonical Allele Identifier: CA388786421

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773059T>C (hg19) ; chr13:g.113118745T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118745T>C , CM000675.2:g.113118745T>C	GRCh38
NC_000013.10:g.113773059T>C , CM000675.1:g.113773059T>C	GRCh37
NC_000013.9:g.112821060T>C	NCBI36
NG_009258.1:g.947T>C , LRG_548:g.947T>C
NG_009262.1:g.17955T>C , LRG_554:g.17955T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1072T>C MANE Select	ENSP00000329546.4:p.Ser358Pro
ENST00000346342.7:c.1072T>C	ENSP00000329546.3:p.Ser358Pro
ENST00000375581.3:c.1138T>C	ENSP00000364731.3:p.Ser380Pro
ENST00000541084.5:c.886T>C	ENSP00000442051.2:p.Ser296Pro
NM_000131.4:c.1138T>C , LRG_554t1:c.1138T>C	NP_000122.1:p.Ser380Pro
NM_001267554.1:c.886T>C	NP_001254483.1:p.Ser296Pro
NM_019616.3:c.1072T>C , LRG_554t2:c.1072T>C	NP_062562.1:p.Ser358Pro
NR_051961.1:n.1159T>C
XM_006719963.2:c.931T>C	XP_006720026.1:p.Ser311Pro
XM_011537474.1:c.1180T>C	XP_011535776.1:p.Ser394Pro
XM_011537475.1:c.994T>C	XP_011535777.1:p.Ser332Pro
XM_011537476.1:c.832T>C	XP_011535778.1:p.Ser278Pro
XM_011537477.1:c.1141T>C	XP_011535779.1:p.Ser381Pro
XM_006719963.3:c.976T>C	XP_006720026.2:p.Ser326Pro
XM_011537474.2:c.1225T>C	XP_011535776.2:p.Ser409Pro
XM_011537475.2:c.1039T>C	XP_011535777.2:p.Ser347Pro
XM_011537476.2:c.832T>C	XP_011535778.1:p.Ser278Pro
NM_019616.4:c.1072T>C MANE Select	NP_062562.1:p.Ser358Pro
NR_051961.2:n.1156T>C
NM_001267554.2:c.886T>C	NP_001254483.1:p.Ser296Pro