Canonical Allele Identifier: CA2336427171

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354704C= , CM000681.2:g.41354704C= GRCh38
NC_000019.9:g.41860609C= , CM000681.1:g.41860609C= GRCh37
NC_000019.8:g.46552449C= NCBI36
NG_013091.1:g.14470G=
NG_013364.1:g.4223G=

Transcript Alleles

HGVS Amino-acid change
ENST00000243578.8:c.524G= (B9D2) MANE Select ENSP00000243578.2:p.Cys175=
ENST00000675972.1:c.524G= (B9D2) ENSP00000501911.1:p.Cys175=
ENST00000243578.7:c.524G= (B9D2) ENSP00000243578.2:p.Cys175=
ENST00000539627.5:c.-30+3502C= (TMEM91) ENSP00000441900.1:n.-30+3502C=
ENST00000594416.1:c.*370G= (B9D2) ENSP00000469666.1:n.*370G=
ENST00000604123.5:c.142+389C= (TMEM91) ENSP00000474871.1:n.142+389C=
ENST00000604424.1:n.350+3502C=
NM_030578.3:c.524G= (B9D2) NP_085055.2:p.Cys175=
XM_006723405.1:c.398G= (B9D2) XP_006723468.1:p.Cys133=
XM_011527349.1:c.524G= (B9D2) XP_011525651.1:p.Cys175=
XM_011527350.1:c.365G= (B9D2) XP_011525652.1:p.Cys122=
XM_011527349.2:c.524G= (B9D2) XP_011525651.1:p.Cys175=
XM_011527350.2:c.365G= (B9D2) XP_011525652.1:p.Cys122=
NM_030578.4:c.524G= (B9D2) MANE Select NP_085055.2:p.Cys175=