Canonical Allele Identifier: CA400191435
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185804A>G , CM000679.2:g.50185804A>G GRCh38
NC_000017.10:g.48263165A>G , CM000679.1:g.48263165A>G GRCh37
NC_000017.9:g.45618164A>G NCBI36
NG_007400.1:g.20836T>C , LRG_1:g.20836T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4222T>C MANE Select ENSP00000225964.6:p.Tyr1408His
ENST00000225964.9:c.4222T>C ENSP00000225964.5:p.Tyr1408His
NM_000088.3:c.4222T>C , LRG_1t1:c.4222T>C NP_000079.2:p.Tyr1408His
XM_005257058.3:c.3952T>C XP_005257115.2:p.Tyr1318His
XM_005257059.3:c.3304T>C XP_005257116.2:p.Tyr1102His
XM_011524341.1:c.4024T>C XP_011522643.1:p.Tyr1342His
XM_005257058.4:c.3952T>C XP_005257115.2:p.Tyr1318His
XM_005257059.4:c.3304T>C XP_005257116.2:p.Tyr1102His
NM_000088.4:c.4222T>C MANE Select NP_000079.2:p.Tyr1408His