Canonical Allele Identifier: CA372063908
Community Standard Title: NM_014112.5(TRPS1):c.2930A>G (p.Asn977Ser)
Gene: TRPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.115414978T>C , CM000670.2:g.115414978T>C GRCh38
NC_000008.10:g.116427206T>C , CM000670.1:g.116427206T>C GRCh37
NC_000008.9:g.116496382T>C NCBI36
NG_012383.3:g.259024A>G

Transcript Alleles

HGVS Amino-acid Change
NM_014112.5:c.2930A>G MANE Select NP_054831.2:p.Asn977Ser
ENST00000395715.8:c.2930A>G MANE Select ENSP00000379065.3:p.Asn977Ser
NM_001282902.2:c.2903A>G NP_001269831.1:p.Asn968Ser
NM_001282902.3:c.2903A>G NP_001269831.1:p.Asn968Ser
NM_001282903.2:c.2909A>G NP_001269832.1:p.Asn970Ser
NM_001282903.3:c.2909A>G NP_001269832.1:p.Asn970Ser
NM_001330599.1:c.2891A>G NP_001317528.1:p.Asn964Ser
NM_001330599.2:c.2891A>G NP_001317528.1:p.Asn964Ser
NM_014112.4:c.2930A>G NP_054831.2:p.Asn977Ser
ENST00000220888.9:c.2891A>G ENSP00000220888.5:p.Asn964Ser
ENST00000395715.7:c.2930A>G ENSP00000379065.3:p.Asn977Ser
ENST00000518018.1:c.264A>G
ENST00000519076.5:c.2153A>G ENSP00000428910.1:p.Asn718Ser
ENST00000520276.5:c.2903A>G ENSP00000428680.1:p.Asn968Ser
ENST00000640765.1:c.2891A>G ENSP00000492037.1:p.Asn964Ser
XM_005251049.2:c.2891A>G XP_005251106.1:p.Asn964Ser
XM_006716625.1:c.2930A>G XP_006716688.1:p.Asn977Ser
XM_011517264.1:c.2930A>G XP_011515566.1:p.Asn977Ser
XM_011517264.2:c.2930A>G XP_011515566.1:p.Asn977Ser
XM_011517265.1:c.2930A>G XP_011515567.1:p.Asn977Ser
XM_011517266.1:c.2930A>G XP_011515568.1:p.Asn977Ser
XM_011517266.3:c.2930A>G XP_011515568.1:p.Asn977Ser
XM_011517267.1:c.2909A>G XP_011515569.1:p.Asn970Ser
XM_011517268.1:c.2891A>G XP_011515570.1:p.Asn964Ser
XM_011517268.2:c.2891A>G XP_011515570.1:p.Asn964Ser