Canonical Allele Identifier: CA1479897684
Gene: ADH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99208528C= , CM000666.2:g.99208528C= GRCh38
NC_000004.11:g.100129685C= , CM000666.1:g.100129685C= GRCh37
NC_000004.10:g.100348708C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000237653.11:c.828+140G= ENSP00000237653.7:n.828+140G=
ENST00000394897.5:c.828+140G= ENSP00000378358.1:n.828+140G=
ENST00000394899.6:c.828+140G= MANE Select ENSP00000378359.2:n.828+140G=
ENST00000504257.1:n.611G=
ENST00000507484.5:c.*292+140G= ENSP00000425275.1:n.*292+140G=
ENST00000508558.1:c.636+140G= ENSP00000426187.1:n.636+140G=
ENST00000512708.5:c.147+140G= ENSP00000422124.1:n.147+140G=
NM_000672.3:c.828+140G= NP_000663.1:n.828+140G=
NM_001102470.1:c.828+140G= NP_001095940.1:n.828+140G=
NR_037884.1:n.3789+4097C=
NR_132990.1:n.563+140G=
XM_005262731.2:c.828+140G= XP_005262788.2:n.828+140G=
XR_244619.2:n.919+140G=
NM_001102470.2:c.828+140G= MANE Select NP_001095940.1:n.828+140G=
NM_000672.4:c.828+140G= NP_000663.1:n.828+140G=
NR_132990.2:n.563+140G=