Canonical Allele Identifier: CA400200183
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188128G>C , CM000679.2:g.50188128G>C GRCh38
NC_000017.10:g.48265489G>C , CM000679.1:g.48265489G>C GRCh37
NC_000017.9:g.45620488G>C NCBI36
NG_007400.1:g.18512C>G , LRG_1:g.18512C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3229C>G MANE Select ENSP00000225964.6:p.Pro1077Ala
ENST00000225964.9:c.3229C>G ENSP00000225964.5:p.Pro1077Ala
ENST00000486572.1:n.427C>G
ENST00000511732.1:n.553C>G
NM_000088.3:c.3229C>G , LRG_1t1:c.3229C>G NP_000079.2:p.Pro1077Ala
XM_005257058.3:c.2959C>G XP_005257115.2:p.Pro987Ala
XM_005257059.3:c.2311C>G XP_005257116.2:p.Pro771Ala
XM_011524341.1:c.3031C>G XP_011522643.1:p.Pro1011Ala
XM_005257058.4:c.2959C>G XP_005257115.2:p.Pro987Ala
XM_005257059.4:c.2311C>G XP_005257116.2:p.Pro771Ala
NM_000088.4:c.3229C>G MANE Select NP_000079.2:p.Pro1077Ala