Canonical Allele Identifier: CA467654483
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137591789A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134699943A>G , CM000671.2:g.134699943A>G GRCh38
NC_000009.11:g.137591789A>G , CM000671.1:g.137591789A>G GRCh37
NC_000009.10:g.136731610A>G NCBI36
NG_008030.1:g.63138A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371820.4:c.312A>G ENSP00000360885.4:p.Thr104=
ENST00000371817.8:c.312A>G MANE Select ENSP00000360882.3:p.Thr104=
ENST00000371817.7:c.312A>G ENSP00000360882.3:p.Thr104=
ENST00000464187.1:n.734A>G
ENST00000618395.4:c.312A>G ENSP00000481360.1:p.Thr104=
NM_000093.4:c.312A>G NP_000084.3:p.Thr104=
NM_001278074.1:c.312A>G NP_001265003.1:p.Thr104=
XR_929712.1:n.714A>G
XR_929713.1:n.714A>G
XM_017014266.2:c.312A>G XP_016869755.1:p.Thr104=
XR_001746183.1:n.710A>G
NM_000093.5:c.312A>G MANE Select NP_000084.3:p.Thr104=