Canonical Allele Identifier: CA270012523
Community Standard Title: NM_153700.2(STRC):c.876-140C>T
Gene: STRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43616830G>A , CM000677.2:g.43616830G>A GRCh38
NC_000015.9:g.43909028G>A , CM000677.1:g.43909028G>A GRCh37
NC_000015.8:g.41696320G>A NCBI36
NG_011636.1:g.6971C>T

Transcript Alleles

HGVS Amino-acid Change
NM_153700.2:c.876-140C>T MANE Select NP_714544.1:n.876-140C>T
ENST00000450892.7:c.876-140C>T MANE Select ENSP00000401513.2:n.876-140C>T
ENST00000428650.5:c.876-140C>T ENSP00000415991.1:n.876-140C>T
ENST00000432436.1:c.696-140C>T ENSP00000407303.1:n.696-140C>T
ENST00000440125.5:c.876-140C>T ENSP00000394866.1:n.876-140C>T
ENST00000450892.6:c.876-140C>T ENSP00000401513.2:n.876-140C>T
ENST00000541030.5:c.-1234-140C>T ENSP00000440413.1:n.-1234-140C>T
ENST00000643290.1:c.1201-140C>T ENSP00000495476.1:n.1201-140C>T
XM_011521277.1:c.1365-140C>T XP_011519579.1:n.1365-140C>T
XM_011521278.1:c.903-140C>T XP_011519580.1:n.903-140C>T
XM_011521279.1:c.903-140C>T XP_011519581.1:n.903-140C>T