Canonical Allele Identifier: CA388786581

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773097C>G (hg19) ; chr13:g.113118783C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118783C>G , CM000675.2:g.113118783C>G	GRCh38
NC_000013.10:g.113773097C>G , CM000675.1:g.113773097C>G	GRCh37
NC_000013.9:g.112821098C>G	NCBI36
NG_009258.1:g.985C>G , LRG_548:g.985C>G
NG_009262.1:g.17993C>G , LRG_554:g.17993C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.1110C>G MANE Select	ENSP00000329546.4:p.Tyr370Ter
ENST00000346342.7:c.1110C>G	ENSP00000329546.3:p.Tyr370Ter
ENST00000375581.3:c.1176C>G	ENSP00000364731.3:p.Tyr392Ter
ENST00000541084.5:c.924C>G	ENSP00000442051.2:p.Tyr308Ter
NM_000131.4:c.1176C>G , LRG_554t1:c.1176C>G	NP_000122.1:p.Tyr392Ter
NM_001267554.1:c.924C>G	NP_001254483.1:p.Tyr308Ter
NM_019616.3:c.1110C>G , LRG_554t2:c.1110C>G	NP_062562.1:p.Tyr370Ter
NR_051961.1:n.1197C>G
XM_006719963.2:c.969C>G	XP_006720026.1:p.Tyr323Ter
XM_011537474.1:c.1218C>G	XP_011535776.1:p.Tyr406Ter
XM_011537475.1:c.1032C>G	XP_011535777.1:p.Tyr344Ter
XM_011537476.1:c.870C>G	XP_011535778.1:p.Tyr290Ter
XM_011537477.1:c.1179C>G	XP_011535779.1:p.Tyr393Ter
XM_006719963.3:c.1014C>G	XP_006720026.2:p.Tyr338Ter
XM_011537474.2:c.1263C>G	XP_011535776.2:p.Tyr421Ter
XM_011537475.2:c.1077C>G	XP_011535777.2:p.Tyr359Ter
XM_011537476.2:c.870C>G	XP_011535778.1:p.Tyr290Ter
NM_019616.4:c.1110C>G MANE Select	NP_062562.1:p.Tyr370Ter
NR_051961.2:n.1194C>G
NM_001267554.2:c.924C>G	NP_001254483.1:p.Tyr308Ter