Canonical Allele Identifier: CA2838302317

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44080270A>T , CM000679.2:g.44080270A>T GRCh38
NC_000017.10:g.42157638A>T , CM000679.1:g.42157638A>T GRCh37
NC_000017.9:g.39513164A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696392.1:c.*275A>T (G6PC3) ENSP00000512602.1:n.*275A>T
ENST00000682912.1:c.2826-45T>A (HDAC5) MANE Select ENSP00000507606.1:n.2826-45T>A
ENST00000225983.10:c.2829-45T>A (HDAC5) ENSP00000225983.5:n.2829-45T>A
ENST00000336057.9:c.2571-45T>A (HDAC5) ENSP00000337290.4:n.2571-45T>A
ENST00000586802.5:c.2826-45T>A (HDAC5) ENSP00000468004.1:n.2826-45T>A
NM_001015053.1:c.2829-45T>A (HDAC5) NP_001015053.1:n.2829-45T>A
NM_005474.4:c.2826-45T>A (HDAC5) NP_005465.2:n.2826-45T>A
XM_005256904.3:c.2829-45T>A (HDAC5) XP_005256961.1:n.2829-45T>A
XM_005256905.1:c.2826-45T>A (HDAC5) XP_005256962.1:n.2826-45T>A
XM_005256906.3:c.2826-45T>A (HDAC5) XP_005256963.1:n.2826-45T>A
XM_005256907.1:c.2814-45T>A (HDAC5) XP_005256964.1:n.2814-45T>A
XM_011524149.1:c.2802-45T>A (HDAC5) XP_011522451.1:n.2802-45T>A
XM_011524150.1:c.2799-45T>A (HDAC5) XP_011522452.1:n.2799-45T>A
XM_011524151.1:c.2703-45T>A (HDAC5) XP_011522453.1:n.2703-45T>A
XR_934338.1:n.3158+131T>A (HDAC5)
XM_005256905.2:c.2826-45T>A (HDAC5) XP_005256962.1:n.2826-45T>A
XM_005256906.4:c.2826-45T>A (HDAC5) XP_005256963.1:n.2826-45T>A
XM_011524149.2:c.2802-45T>A (HDAC5) XP_011522451.1:n.2802-45T>A
XM_017023988.1:c.2943-45T>A (HDAC5) XP_016879477.1:n.2943-45T>A
XM_017023989.1:c.2943-45T>A (HDAC5) XP_016879478.1:n.2943-45T>A
XM_017023990.1:c.2940-45T>A (HDAC5) XP_016879479.1:n.2940-45T>A
XM_017023991.1:c.2940-45T>A (HDAC5) XP_016879480.1:n.2940-45T>A
XM_017023992.1:c.2928-45T>A (HDAC5) XP_016879481.1:n.2928-45T>A
XM_017023993.1:c.2916-45T>A (HDAC5) XP_016879482.1:n.2916-45T>A
XM_017023996.1:c.2703-45T>A (HDAC5) XP_016879485.1:n.2703-45T>A
NM_001015053.2:c.2829-45T>A (HDAC5) NP_001015053.1:n.2829-45T>A
NM_005474.5:c.2826-45T>A (HDAC5) MANE Select NP_005465.2:n.2826-45T>A
NM_001382393.1:c.2826-45T>A (HDAC5) NP_001369322.1:n.2826-45T>A