Canonical Allele Identifier: CA400195828
Community Standard Title: NM_000088.4(COL1A1):c.3814+2T>C
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186638A>G , CM000679.2:g.50186638A>G GRCh38
NC_000017.10:g.48263999A>G , CM000679.1:g.48263999A>G GRCh37
NC_000017.9:g.45618998A>G NCBI36
NG_007400.1:g.20002T>C , LRG_1:g.20002T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3814+2T>C MANE Select NP_000079.2:n.3814+2T>C
ENST00000225964.10:c.3814+2T>C MANE Select ENSP00000225964.6:n.3814+2T>C
NM_000088.3:c.3814+2T>C , LRG_1t1:c.3814+2T>C NP_000079.2:n.3814+2T>C
ENST00000225964.9:c.3814+2T>C ENSP00000225964.5:n.3814+2T>C
ENST00000510710.3:n.483+2T>C
XM_005257058.3:c.3544+2T>C XP_005257115.2:n.3544+2T>C
XM_005257058.4:c.3544+2T>C XP_005257115.2:n.3544+2T>C
XM_005257059.3:c.2896+2T>C XP_005257116.2:n.2896+2T>C
XM_005257059.4:c.2896+2T>C XP_005257116.2:n.2896+2T>C
XM_011524341.1:c.3616+2T>C XP_011522643.1:n.3616+2T>C