Canonical Allele Identifier: CA400204465
Community Standard Title: NM_000088.4(COL1A1):c.2938-2A>G
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50189012T>C , CM000679.2:g.50189012T>C GRCh38
NC_000017.10:g.48266373T>C , CM000679.1:g.48266373T>C GRCh37
NC_000017.9:g.45621372T>C NCBI36
NG_007400.1:g.17628A>G , LRG_1:g.17628A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2938-2A>G MANE Select NP_000079.2:n.2938-2A>G
ENST00000225964.10:c.2938-2A>G MANE Select ENSP00000225964.6:n.2938-2A>G
NM_000088.3:c.2938-2A>G , LRG_1t1:c.2938-2A>G NP_000079.2:n.2938-2A>G
ENST00000225964.9:c.2938-2A>G ENSP00000225964.5:n.2938-2A>G
XM_005257058.3:c.2668-2A>G XP_005257115.2:n.2668-2A>G
XM_005257058.4:c.2668-2A>G XP_005257115.2:n.2668-2A>G
XM_005257059.3:c.2020-2A>G XP_005257116.2:n.2020-2A>G
XM_005257059.4:c.2020-2A>G XP_005257116.2:n.2020-2A>G
XM_011524341.1:c.2740-2A>G XP_011522643.1:n.2740-2A>G