Canonical Allele Identifier: CA467656901

Gene: COL5A1

Linked Data

• MyVariant Identifiers: chr9:g.137697018A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134805172A>T , CM000671.2:g.134805172A>T	GRCh38
NC_000009.11:g.137697018A>T , CM000671.1:g.137697018A>T	GRCh37
NC_000009.10:g.136836839A>T	NCBI36
NG_008030.1:g.168367A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371820.4:c.3216A>T	ENSP00000360885.4:p.Gly1072=
ENST00000371817.8:c.3216A>T MANE Select	ENSP00000360882.3:p.Gly1072=
ENST00000371817.7:c.3216A>T	ENSP00000360882.3:p.Gly1072=
ENST00000618395.4:c.3216A>T	ENSP00000481360.1:p.Gly1072=
NM_000093.4:c.3216A>T	NP_000084.3:p.Gly1072=
NM_001278074.1:c.3216A>T	NP_001265003.1:p.Gly1072=
XR_929712.1:n.3618A>T
XR_929713.1:n.3618A>T
XM_017014266.2:c.3216A>T	XP_016869755.1:p.Gly1072=
XR_001746183.1:n.3614A>T
NM_000093.5:c.3216A>T MANE Select	NP_000084.3:p.Gly1072=